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Conferences on Medical device (past events)

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Showing 2197 conferences
Medical Device R&D Summit
Mar 2025
International Experts Summit on Biomedical Engineering and Systems
Mar 2025
World Radiology and Medical Imaging Conference (WRMI)
Mar 2025
World Congress on Cardiology and Cardiovascular Therapeutics
Feb 2025
MedDev AI Marketing Summit
Feb 2025
Corporate Compliance & Transparency In Life Sciences
Feb 2025
SOP Writing, Training and Compliance in the Pharmaceutical Industry
Feb 2025
KOL & MSL Excellence Summit
Feb 2025
Digital Strategy & Innovation for Medical Affairs Summit
Feb 2025
ICBAB : International Conference on Biotherapeutics Analytical and Bioinnovation
Feb 2025
Enterprise Architecture in Life Sciences and Healthcare Forum
Feb 2025
Hematology and Medical Oncology Practice Updates and Board Review
Feb 2025
Microfluidics Consortium Open Day
Jan 2025
Risk-Based Quality Management Summit
Jan 2025
World Congress on Spine and Spinal Disorders
Dec 2024
Patient Recruitment for Rare Disease Trials Summit
Dec 2024
International Conference on Spine and Spinal Disorders
Dec 2024
World Congress on Biomaterials, Biomedical Applications & Nanomedicine
Dec 2024
Cell and Gene Therapy Medical Affairs Summit
Dec 2024
Pharmaceutical and Medical Meeting Planners Summit
Dec 2024
Global Conference on Pharmaceutical and Clinical Research
Nov 2024
International Conference on Clinical Research and Clinical Trials
Nov 2024
Congress on Cardiology and Cardiac Surgery
Nov 2024
International Society for Telemedicine & eHealth (ISfTeH) International Conference
Nov 2024
International Conference on Traditional & Alternative Medicine
Nov 2024
International Conference on Cell Science & Molecular Biology
Nov 2024
Asian Conference on Innovative Therapies for Diabetes Management (ATTD-ASIA)
Nov 2024
International Pharma Congress
Nov 2024
International Conference on Biomaterials and Biodevices
Nov 2024
International K-Beauty Fresh Cadaver Workshop
Nov 2024
Dental Summit
Nov 2024
Audits - Self/Internal, Vendor and Regulatory Inspections
Nov 2024
Next-Gen MSL Excellence Summit
Nov 2024
Investigator-Initiated Trials
Nov 2024
Drafting and Negotiating Clinical Trial Agreements
Nov 2024
International Conference on Telemedicine & Digital Health
Oct 2024
AstanaZdorovie
Oct 2024
Pharma India Expo
Oct 2024
International Conference on Orthopedics, Arthroplasty and Rheumatology
Oct 2024
Global Research Conference on Medical, Medicine and Health Sciences (GRCMED)
Oct 2024
Global Conference on Biosensors
Oct 2024
Leachables and Extractables MasterClass - EU
Oct 2024
International Conference on Telemedicine and Digital Health
Sep 2024
Global Research Conference on Equipments and Technologies for Medical and Surgery (GRCSURG)
Sep 2024
Post-Authorisation Safety Studies MasterClass- EU
Sep 2024
International Meet on Stemcells and Regenerative Medicine (STEMCELLSMEET)
Sep 2024
International Conference on Dentistry and Craniofacial Research
Sep 2024
Aseptic Processing Technology
Sep 2024
Optimizing Hybrid Clinical Trials Summit
Sep 2024
Pre Filled Syringes Connect
Sep 2024
ADC and Radiopharmaceuticals Pharma and Biotech Partnering Summit
Sep 2024
Global Conference on Medical and Health Science (GCMHS)
Sep 2024
SolGel International Conference
Sep 2024
International Conference on Pharmaceutics, Formulations & Drug Delivery Systems
Aug 2024
Global Pharmacovigilance & Clinical Trials Summit
Jul 2024
International Conference on Cardiovascular Medicine and Cardiac Surgery
Jun 2024
International Congress on Advances in Clinical Research & Trials
Jun 2024
Pre-Filled Syringes and Injectables Summit
Jun 2024
World Congress on Virtual Rehabilitation
Jun 2024
World Congress on Cardiology and Heart Failure
May 2024
Clinical Operations and Clinical Trial Supply Chain Strategy Meeting
May 2024
China Consumer Health Digital Innovation Summit
May 2024
Global Meet on Pharmaceutics and Drug Delivery Systems (GMPDDS)
May 2024
Health Equity in Clinical Trials Congress
May 2024
Re:Imagine Medical Device Marketing
Apr 2024
Global Biotechnology Congress
Apr 2024
MEDEXPO Africa
Apr 2024
World Congress on Anesthesia and Pain Medicine
Apr 2024
Clinical Trial Billing and Research Compliance Summit
Mar 2024
asiaPLX - The Marketplace for Pharma Business Opportunities
Mar 2024
Clinical Trials Festival Asia
Mar 2024
Trial Master File (TMF) Summit
Mar 2024
The KSKCS & KCCS International Conference
Mar 2024
Medical Affairs and Scientific Communications Forum
Mar 2024
MarketsandMarkets Biomarker and Companion Diagnostics Conference UK/EU
Mar 2024
Odisha Medical Expo
Feb 2024
Interventional Cardiology Skills Enhancement Course
Feb 2024
Applied Nanotechnology Summit
Dec 2023
Clinical Trial Regulation MasterClass
Dec 2023
International Conferences on Pharmacology and Clinical Trial
Dec 2023
Warsaw Medical Expo
Dec 2023
GCP Inspection Readiness
Dec 2023
Emirates International Orthopedic Congress
Nov 2023
World Congress on Industrial Biotechnology
Nov 2023
Medical Devices and IVD Conference
Nov 2023
World Congress On Pharmaceutical Research and Drug Discovery
Nov 2023
SAHARA+ Conference
Nov 2023
European Conference on Advance Clinical Trials and Research
Nov 2023
Implementation of a Successful Technology Transfer Process
Nov 2023
ADSCC Bone Marrow Transplant & Cellular Therapy Congress
Nov 2023
Global Summit on Heart and Cardiovascular Care
Nov 2023
EMT - European Medical Tourism
Nov 2023
Next Generation Gene Therapeutics
Nov 2023
5G Telemedicine Security Conference
Nov 2023
Injectables Summit
Oct 2023
Global Forum (GF) on Temperature Controlled Life Sciences Supply Chains
Oct 2023
Disposable Solutions for Biomanufacturing Global
Oct 2023
MarketsandMarkets Biomarker and Companion Diagnostics Conference
Oct 2023
International Medical Exhibition - Public Health
Oct 2023
International Specialized Exhibition Clean Rooms Technologies CleanTechExpo
Oct 2023
World Congress on Drug Innovation (WCDI)
Oct 2023
iMED Medical Equipment Exhibition (iMed)
Oct 2023
Middle East Cardiovascular Pharmacotherapy Forum
Oct 2023
MarketsandMarkets Biomarker and Companion Diagnostics Conference
Oct 2023
Software Design for Medical Devices (SDMD) Global
Sep 2023
International Medical Forum (IMF)
Sep 2023
International Conference on Clinical Trials
Sep 2023
Data Driven Approach in Clinical Trials
Sep 2023
American Medical Device Summit
Sep 2023
European congress on Biomaterials and Bio-devices (ECBIOMAT)
Sep 2023
International conference on Pharmaceutics and Novel Drug Delivery Systems
Sep 2023
Smart(er) Biomanufacturing: Evaluating the Risks and Opportunities
Sep 2023
Finance & Accounting for Bioscience Companies
Sep 2023
LSX World Congress - Biotech | Healthtech | Medtech
Sep 2023
International Conference on Oncology and Precision Medicine
Sep 2023
Philippines Laboratory Expo
Aug 2023
McGill@Whistler Implant Symposium
Aug 2023
Sri Lanka Medical Association (SLMA) International Medical Congress
Jul 2023
Advanced Wound Care Summit US
Jul 2023
FDA`s Medical Device Software Regulation Strategy
Jun 2023
JAK Inhibitors Drug Development Summit
Jun 2023
Medical Device Manufacturing and R&D Summit
Jun 2023
Global Congress on Medical & Clinical Case Reports
Jun 2023
Medical Writing & Communication Strategy
May 2023
Pharmaceutical and Medical Device Ethics and Compliance Congress
May 2023
China Med - The International Medical Instruments & Equipment Exhibition
May 2023
International Conference on Clinical Research
May 2023
Clinical Trials Quality & Inspection Updates
May 2023
PEGS Boston Conference & Expo
May 2023
LVPEI Startup Challenge
Apr 2023
Effective Project Management For Clinical Trials
Mar 2023
MarketsandMarkets PathDx
Mar 2023
Pharma & Biotech R&D Portfolio Management In The Century
Mar 2023
International Conference on Medical, Biological and Pharmaceutical Sciences (ICMBPS)
Mar 2023
Future Health
Mar 2023
The Hermina International Conference on Health (HICH)
Feb 2023
The Veterinary Drug Approval Process and FDA Regulatory Oversight
Feb 2023
Clinical Data Disclosure and Transparency Summit
Feb 2023
International Congress on Biomedical and Bio Instrumentation (ICBBI)
Feb 2023
Life Sciences, Clinical Trials, Patient Recruitment & Retention
Jan 2023
Latin America - Understanding Regulatory Compliance Requirements Across the Life Science Industry (Pharmaceuticals, Biologics, Medical Devices, IVDs)
Dec 2022
World Conference on Pharma Industry and Medical Devices
Dec 2022
Biomanufacturing Conference Asia
Dec 2022
Pharma and Device Packaging and Labeling West Coast
Nov 2022
International Conference on Drug Discovery and Drug Development
Nov 2022
Technical Documentation to Comply with the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation)
Nov 2022
Field Service Connect
Nov 2022
International Conference on Advanced Pharmacy and Clinical Research
Nov 2022
ENDOCLUBNORD
Nov 2022
World Congress On Biopolymers & Bioplastics
Oct 2022
Accelerating Clinical Trials in Asia
Oct 2022
Clinical Trials Summit
Oct 2022
International Congress on Transplantation and Medical Surgery
Oct 2022
Xcelerate at Biotech Week Boston
Sep 2022
Nanosphere UAE
Sep 2022
RAS Targeted Drug Development Summit
Sep 2022
International Conference on Medical and Health sciences
Sep 2022
International Conference on Healthcare Engineering (ICHE)
Sep 2022
Fierce Biotech Summit
Sep 2022
PK/PD in Drug Discovery and Development for the US market MasterClass
Sep 2022
Pharma Summit : Drug Discovery & Community Trial
Aug 2022
Global Summit on Digital Healthcare and Future Medical Technologies
Aug 2022
International Conference on Medical Case Reports
Aug 2022
International Conference on Clinical Trials and Clinical Research
Aug 2022
WYN Cardiology Forum
Jul 2022
Analytical Instrument Qualification & Validation - Use of Excel and FDA Audit Preparation
Jul 2022
Pre Event Respiratory Drugs
Jun 2022
Combination Products Summit
Jun 2022
ISPOR Summit
May 2022
Medical Device Regulations & Compliance Summit
May 2022
Convergence
May 2022
International Conference on Clinical Case Reports
May 2022
U.S. FDA and EU Medical Device Directive Requirements for DHFs, DMRs, DHRs, and TF/DDs
May 2022
Understanding and Implementing a Quality by Design (QbD) Program
May 2022
Personalized and Precision Medicine International Conference (PEMED)
Apr 2022
MedTech Korea Summit
Apr 2022
Injectable Drug Delivery
Mar 2022
World EPA Congress
Mar 2022
European Congress on Vaccines R&D & Vaccination
Mar 2022
3-Hour Virtual Seminar on IQ, OQ, PQ in the Verification and Validation Process
Mar 2022
Robotics and Automation in Pharma Conference
Feb 2022
The EAAR Conference on New Medical Device Regulations (RMD2022)
Feb 2022
EC Medical Devices Vigilance System and Post Marketing Surveillance
Jan 2022
Medical Device Biocompatibility and Toxicology
Jan 2022
Speaker Programs and Advisory Boards
Jan 2022
UCG on Diabetes and Endocrinology Conference
Jan 2022
EMIS National User Group Conference (EMIS NUG)
Dec 2021
FDA/CMS Summit
Dec 2021
Clinical Trial Innovation Summit
Dec 2021
Global UDI and Master Data Forum
Dec 2021
Cleaning Validation for Pharma
Dec 2021
FDA Pharmaceutical Labeling Boot Camp
Dec 2021
LogiMed
Dec 2021
World Congress on Ophthalmology and Eye Disorders
Nov 2021
Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices
Nov 2021
Inhalation & Respiratory Drug Products Summit
Nov 2021
Aesthetic & Cosmetic Regulatory Events Summit (ACRAS)
Nov 2021
Regulatory and Technology Considerations for the Design of Medical Device Software MasterClass
Nov 2021
Vendor/CRO Management and Oversight MasterClass
Nov 2021
Global Pharmaceutical and Medical Meetings Summit
Oct 2021
Drug Delivery Partnerships
Oct 2021
Point-of-Care Diagnostics, Global Health & Biosensors World Congress
Oct 2021
ICBE : International Conference on Biomedical Engineering
Oct 2021
Medical Device Digi Expo
Oct 2021
BODYNETS - EAI International Conference on Body Area Networks
Oct 2021
New Medical Device Regulation
Oct 2021
Medical Devices Innovation Programme
Oct 2021
International Congress of Hearing Aid Acousticians (EUHA)
Oct 2021
Combination Products Summit
Oct 2021
Pharma Packaging and Labelling Europe
Sep 2021
Data Integrity: FDA/EU Requirements and Implementation
Sep 2021
Precision Medicine World Conference Pittsburgh (PMWC)
Sep 2021
International Conference on Digital Pathology
Sep 2021
National - Strategy Summit on Paragraph IV Litigation
Sep 2021
Advanced Precision Medicine MasterClass
Sep 2021
Digital Marketing for Medical Devices
Aug 2021
Pharma CMI - Competitive Market Intelligence
Aug 2021
ComplianceOnline Medical Device Summit
Aug 2021
National Institute for Health and Care Excellence (NICE), UK: Transformation in Action
Aug 2021
International Conference on Ergonomics and Human Factors
Jul 2021
International Conference on Cancer Science and Therapy
Jul 2021
Breakthroughs Conference and Exhibition
Jun 2021
Risk Management in Medical Devices Industry
Jun 2021
Digital Transformation Journey for Medical Affairs
Jun 2021
Bangladesh Medical & Healthcare Virtual Expo
Jun 2021
Decoding Digital Health for Life Sciences
Jun 2021
Clinical Trials Innovation Programme
May 2021
Clinical Trials Inspection Readiness Summit
May 2021
Conference on 3D Printing in Medicine
May 2021
Digital Marketing for Medical Devices West
Apr 2021
Drug/Device Combination Products Summit
Apr 2021
World Congress on Healthcare Management System
Apr 2021
MedDevice Ignition
Mar 2021
Sri Lanka Medical & Equipment Virtual Expo
Mar 2021
Supply Chain Re-Innovation: Life Sciences
Mar 2021
Drug Delivery Devices Symposium
Mar 2021
Ventricular Assist Device (VAD) CME Symposium for Community Partners
Feb 2021
International Conference on Clinical Trials
Feb 2021
International Conference on Sustainable Modern Advance in Research and Technology
Jan 2021
Content Marketing for Life Sciences
Dec 2020
The International Conference on Biological Therapy (ICBT)
Dec 2020
Clinical Performance Metrics and Analytics Summit
Dec 2020
FDA`s GMP Expectations for Phase IV and -in-Man Clinical Trials
Dec 2020
World Congress on Advances in Analytical and Bio-Analytical Techniques
Dec 2020
Istanbul Health Expo
Dec 2020
Annual MedTech Access Leaders Forum
Dec 2020
ZDRAVO OKHRANENIYE - Healthcare, Medical Engineering and Pharmaceuticals
Dec 2020
Plenareno Pharma Middle East Congress
Dec 2020
Endpoint Adjudication
Dec 2020
Human Abuse Liability and Abuse-Deterrent Formulations
Nov 2020
International Conference on Medical Imaging and Case Reports (MICR)
Nov 2020
World Biotechnology Congress
Nov 2020
The European Conference on Clinical Studies with Medical Devices and IVDs (CSMD2020)
Nov 2020
The International Conference on Clinical Trials and Regulations of Medical Devices and IVD (CSMD)
Nov 2020
International Conference on Pharmaceutics and Drug Delivery Systems
Nov 2020
Product Complaints and Recalls Virtual Summit
Nov 2020
International Conference on Biomedical Engineering & Instrumentation
Nov 2020
International Congress on Traditional & Alternative Medicine
Nov 2020
International Conference on Biopharma and Biotherapeutics
Oct 2020
Technology Transfer for Biologics Conference
Oct 2020
International Conference on Research and Development in Imaging, Nanotechnology, Industrial Design and Robotics (RDINIDR)
Oct 2020
Essentials Of USP Microbiology - For Those Who Are Not Microbiologists or Who Wish A Refresher
Oct 2020
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering Training
Oct 2020
The Drug Development Process from Concept to Market
Oct 2020
Med-Tech & Med-Cann World Summit
Oct 2020
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2020
DigiHealthSouth - EAI International Conference on Digital Healthcare Technologies for the Global South
Oct 2020
RWE, Market Access, Pricing and Reimbursement Americas
Oct 2020
Azerbaijan International Medical Innovations Exhibition (Medinex)
Oct 2020
Project Management for FDA-Regulated Companies
Oct 2020
AI-ML Clinical Development
Sep 2020
CMO Quality Oversight & Risk Management Summit
Sep 2020
Safety Labeling and Packaging Summit
Sep 2020
The A to Z`s of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals, Biologics, Medical Devices, Cosmetics, and Personal Care Products
Sep 2020
International Patient Experience Summit & Eminence Awards
Sep 2020
FDA Audit, Quality Assurance Practices, Responsibilities and Expectations
Sep 2020
World Congress on Biomarkers
Sep 2020
Virtual ISPOR-FDA Summit
Sep 2020
WIRED Health:Tech
Sep 2020
World Congress on Plasma Chemistry and Plasma Processin
Sep 2020
FWD Pharma
Sep 2020
International Conference on Head and Neck Surgery
Sep 2020
Clinical Trials Inspection Readiness Summit
Aug 2020
MedAffairs Leaders Forum USA
Aug 2020
Disclosure and Transparency for Clinical Data Summit
Aug 2020
International Virtual Conference on Public Health (IVCPH)
Aug 2020
Life Science Regulatory Information Summit
Aug 2020
European Summit on Personalized Medicine and Pharmacogenomics
Aug 2020
International Conference and Exhibition on Biomedical Electronics and Devices
Aug 2020
Global Conference on Pharmaceutics and Pharmacology
Aug 2020
International Congress of The Egyptian Society of Tropical Medicine, Infectious and Parasitic Diseases (ESTIP)
Jul 2020
Biomedical Engineering and Instrumentation Summit (BEIS)
Jul 2020
International Conference On Medical and Nursing Education
Jul 2020
Precision in Clinical Trials Boston
Jul 2020
FT Digital Health Summit Europe
Jun 2020
Partnering with ACOs and IDNs Summit
Jun 2020
KOL/Thought Leader Engagement and Advisory Boards Summit
Jun 2020
Implementing a Bullet Proof Quality System for FDA Audit Success
Jun 2020
Beijing International Rehabilitation & Personal Health Expo
Jun 2020
Technical Writing for Pharma, Biotech and Med Devices
Jun 2020
Scholars World Healthcare Summit
Jun 2020
The International Conference on Clinical Pathology and Diagnostic Techniques (CPDT)
May 2020
CATCH-UP : Annual Review of Advances in Heart Failure, Mechanical Circulatory Support & Transplantation
May 2020
Due Diligence Summit for Life Sciences
May 2020
Medical Device Regulations in Latin America
May 2020
World Medical Nanotechnology Congress and Expo
May 2020
Maximizing Investigator Meetings
May 2020
Pre-filled Syringes & Injectables Devices
May 2020
Digital Quality in Clinical Trials
May 2020
Predictive Analytics World Healthcare
May 2020
International Translational and Regenerative Medicine Conference
Apr 2020
International Conference on Dentistry and Integrated Medicine
Apr 2020
Digital Therapeutics and Clinical Innovation Summit
Apr 2020
Global Congress and Expo on Medical imaging and Case reports
Apr 2020
Adaptive Clinical Trials Symposium
Mar 2020
International Conference on Pancreatic Cancer & Liver Diseases
Mar 2020
Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency
Mar 2020
Product Complaints Forum
Mar 2020
FDA`s New Import Program for - Strict Precision
Mar 2020
Pharma Logi
Mar 2020
International Conference on Emerging Materials and Bio-Devices
Mar 2020
MedAffairs Leaders Forum Europe (Spring)
Mar 2020
Aggregate Spend and Open Payments Conference
Mar 2020
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)
Mar 2020
European nutrition and dietetics conference
Mar 2020
Validation and 21 CFR Part 11 Compliance of Computer Systems
Feb 2020
Annual Technological Advances in Healthcare summit
Feb 2020
The International Colorectal Disease Symposium
Feb 2020
Medexpo Africa (Ethiopia)
Feb 2020
Effective Training Skills and Processes in the Pharma Industry
Feb 2020
EU Medical Device Regulation (MDR) Updated CE Marking Process and ISO 13485: Expectations
Feb 2020
Medical Devices: Regulatory and Compliance Summit
Feb 2020
Quality and GMP Compliance for Virtual Companies (Pharmaceutical, Medical Device & Biologics Industries)
Feb 2020
Human Factors Engineering and Usability Studies Summit
Feb 2020
Clinical Trial Regulatory Requirements
Jan 2020
T3: Trials, Tech and Transformation
Jan 2020
International Conference on Biochemistry & Biophysics
Dec 2019
Regulatory Requirements and Principles for Cleaning Validation
Dec 2019
Impact of Brexit on the Pharma & Medical Device Industries
Dec 2019
Clinical Microbiology Conference
Dec 2019
HR Life Sciences
Dec 2019
Multi-Stakeholder Commercial Model Summit
Dec 2019
Virtual Clinical Trials Conference
Dec 2019
Biostatistics for the Non-Statistician
Nov 2019
MedHealth International trade exhibition - Kenya
Nov 2019
Medical Device Registration and Approval Process for the Pacific Rim
Nov 2019
Biocompatibility for Medical Devices
Nov 2019
Scholars International Conference on Advances in Neurology and Neuropsychiatry
Nov 2019
Investigator-Initiated Trials (IIT) Forum
Nov 2019
MedTech Summit US
Nov 2019
You have a BI Positive or Product Sterility Positive - Now What
Nov 2019
Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection
Nov 2019
eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada
Nov 2019
MedAffairs Leaders Forum Autumn
Nov 2019
Medical Tubing US
Nov 2019
Digital Therapeutics Strategic Partnerships Summit
Nov 2019
Managing Your FDA Inspection: Before, During and After
Nov 2019
Confidentiality of Substance Use Disorder Patient Records; Complying with the New Federal Law 42 CFR Part 2
Nov 2019
Biennial Conference of Nuclear Cardiology Society of India
Oct 2019
Strategic Partnerships for Drug Repurposing Forum
Oct 2019
Combination Products Forum
Oct 2019
Pharmaceutical Microbiology
Oct 2019
World conference on Diabetes and Heart Congress
Oct 2019
Medical Innovation Summit
Oct 2019
International Biochemistry Conference
Oct 2019
Festival of Biologics
Oct 2019
Annual Conference on Hypertension and Cardiovascular Diseases
Oct 2019
International Conference on Clinical Trials and Clinical Research
Oct 2019
Highly Potent Active Pharmaceutical Ingredients Summit
Oct 2019
ISO 13485: Quality Management System for Medical Devices
Sep 2019
Computer System Validation & IT Systems Validation Conference
Sep 2019
Designing and Sustaining New and Existing Product Stability Testing Program
Sep 2019
Health Asia International Exhibition & Conference
Sep 2019
Stability Testing Summit
Sep 2019
Annual Pre-Filled Syringes & Injectables Summit
Sep 2019
Medical Devices Meetings Twente
Sep 2019
Human Factors & User Experience for Medical Device Design
Sep 2019
CDISC Mapping 5: ADAM Models - ADSL, BDS and ADAE
Sep 2019
How to Investigate Environmental Monitoring Excursions
Sep 2019
International conference and Exhibition on Pharmaceutics & Novel drug delivery systems (PHARMACEUTICA)
Sep 2019
Implementing UDI (Unique Device Identification) - Plan Now for Success
Sep 2019
Human Factors Engineering to Satisfy the New IEC 62366-1, -2
Aug 2019
Effective Standard Operating Procedure (SOPs) Development
Aug 2019
Trial Master File (TMF) Institute - Philadelphia
Aug 2019
International Conference on Polymers for Advanced Technologies (PAT)
Aug 2019
Adjustable Rate Mortgage (ARM) Rule
Aug 2019
Effective Supplier Management Programs
Aug 2019
Is Your Medical Device Software 510k Ready
Aug 2019
Plastic and Cosmetic Surgery
Aug 2019
21 CFR Part 11 and Risk Assessment
Jul 2019
Death by CAPA Does your CAPA Program need a CAPA
Jul 2019
Process Validation - Overview of Why and How
Jul 2019
6 Most Common Problems in FDA Software Validation and Verification
Jul 2019
Medical Device Verification & Validation
Jul 2019
Basics of Testing Associated with Sterilization Validation and Routine Processing
Jul 2019
Drug Pricing and Reimbursement Stakeholder Summit
Jul 2019
Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)
Jul 2019
Establishing FDA-Compliant Social Media Practices to Avoid FDA Actions
Jul 2019
International Conference on Clinical Research and Biomarkers
Jul 2019
Scale-Up, Cycle Transfer, and Maximum Throughput Capability for Lyophilized Products
Jul 2019
Risk Management in Medical Devices Industry
Jun 2019
Implants
Jun 2019
Supplier Management for Medical Device Manufacturers
Jun 2019
Biocompatibility Testing for Medical Devices
Jun 2019
Effectively Addressing and Remediating FDA`s Form 483 Findings, Warning Letters and Consent Decree Compliance Issues
Jun 2019
CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations
Jun 2019
Medical Sensors Design Conference
Jun 2019
International Conference on Biomedical and Clinical Research
Jun 2019
ASEAN Conference on 3D Print in Medicine
Jun 2019
FDA Quality System Inspection Technique (QSIT) Audits – Good Preparation Practices
Jun 2019
FDA Off-Label Promotion Guidelines
Jun 2019
Dry Powder Inhalers: Annual Conference
Jun 2019
Power Analysis for Sample Size Calculations
Jun 2019
Annual Biomarker World Congress
Jun 2019
Project Management in Clinical Research
Jun 2019
Canada Meetings on Vascular and Interventional Radiology
Jun 2019
Annual Impurities: Genotoxic and Beyond Summit
Jun 2019
CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process
Jun 2019
BioMedical Sensors & Connected Devices Summit
Jun 2019
International Conference on Clinical Research and Biomarkers
Jun 2019
Medima Krasnodar
May 2019
National Conference And Technology Exhibition On Indian Medical Devices & Plastics Disposables / Implants Industry
May 2019
Supplier and Service Provider Controls: FDA Expectations
May 2019
The International Congress on Clinical Trials for Medical Devices (CTMD)
May 2019
FDA Expectations for 505(b)(2) Regulatory Pathway for New Drugs
May 2019
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs
May 2019
Statistical Techniques for Medical Device Manufacturers
May 2019
FDA Recalls - Before You Start, and After You Finish
May 2019
International Conference on Neuroscience (Neurology)
May 2019
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
May 2019
Analytical Techniques
May 2019
Texting and Mobile Devices in Healthcare - HIPAA and CMS Requirements for Security of PHI
May 2019
The Value of a Human Factors Program
May 2019
Quality by Design (QbD) in Pharmaceutical and Medical Device Manufacturing
May 2019
Excel Spreadsheets: Develop and Validate for 21 CFR Part 11 Compliance
May 2019
Production and Process Controls - Ensuring your medical device conforms to its specifications
May 2019
Design History Files and Technical Files/Design Dossiers - Meeting U.S. FDA CGMPS and the EU`s MDD Requirements
May 2019
Effective Records Management and Document Control for Medical Devices
May 2019
Compliance Measures for Case Managers
May 2019
Edition Regulatory Information Management and Data Quality for Pharma Sector
Apr 2019
Wearable Drug Delivery
Apr 2019
In-Depth Testing of Computer Systems Regulated by FDA
Apr 2019
Essentials of Validation - IQ, OQ, PQ
Apr 2019
Ensuring your Site is Ready for an FDA Inspection
Apr 2019
Risk Management in Clinical Research
Apr 2019
iSRRS - The International Conference on Rapid Response Systems and Medical Emergency Teams
Apr 2019
International Conference on Laser, Optics and Photonics
Apr 2019
Medical Device Laws and Regulations in Asia - Part 2 - India, Japan, and Korea
Apr 2019
Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
Apr 2019
HIPAA and Having a Compliant Front Office
Apr 2019
FDA`s New Import Program for
Apr 2019
HIPAA & The medical practice: Requirements for Privacy, Security and Breach Notification
Apr 2019
510(k) and PMA Refuse to Accept Policy
Apr 2019
ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements
Apr 2019
Why Can`t They get This Done? Addressing Executive Function Breakdowns in Children and Adolescents with ASD
Apr 2019
The International event for the Life Science and Technology Industries (LSIE)
Mar 2019
Current Trends in CyberSecurity Threats to Medical Devices
Mar 2019
Method Development and Validation for Assays Supporting Testing of Biologics
Mar 2019
BIHE Healthcare & Dental Exhibition (Cancelled)
Mar 2019
Pre-Filled Syringes
Mar 2019
Process Challenge Device Development for EO Sterilization
Mar 2019
Medical Device Safety and Reporting Summit
Mar 2019
How to Implement a Quality Management System According ISO 13485?
Mar 2019
FDA Inspections - Do`s and Don`ts
Mar 2019
FT Digital Surgery Summit
Mar 2019
Global Experts Meeting on Frontiers in Nanomedicine and Drug Delivery
Mar 2019
The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs
Mar 2019
Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)? Medical Device Single Audit Program (MDSAP)
Mar 2019
Export Certificate for Medical Devices - Out Your Competition!
Mar 2019
EU and US GMP/GDP – Similarities and Differences
Mar 2019
How to apply ISO 62304 standard in a medical software development project?
Mar 2019
Trial Master File Institute - Frankfurt
Mar 2019
Trends for Computer System Validation, Medical Device Compliance and FDA Enforcement
Mar 2019
3-Hour Virtual Seminar on FDA`s Scrutiny of Social Media Promotion
Mar 2019
How to Implement a Quality Management System According ISO 13485?
Mar 2019
The FDA Inspection: Preparation, Management, and Follow - up
Mar 2019
Good Clinical Data Management Practices
Mar 2019
510(k) Update - How to Format Succinct and Comprehensive 510(k)s
Mar 2019
Medical Device Single Audit Program (MDSAP) - How to implement MDSAP in an existing Quality Management System (QMS)?
Mar 2019
Water System Biofilm Control and Microbial Monitoring Myths
Mar 2019
The New ICH GCP E6 R2 Guideline
Feb 2019
International Cold Chain Management Congress
Feb 2019
annual DPharm Europe: Disruptive Innovations to Advance Clinical Trials
Feb 2019
Medical Device Employee Training - Requirements and Implementation Tips
Feb 2019
505(b)(2) NDAs
Feb 2019
Biomedical Engineering: The Engine of Growth for a better Life
Feb 2019
Establishing a Medical Device Security Program
Feb 2019
International Conference on Artificial Intelligence, Soft Computing and Applications (ICA2SC)
Feb 2019
Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoid Common Mistakes
Feb 2019
Measurement Systems Analysis
Feb 2019
Surviving an FDA Sponsor Inspection - Training for Success
Feb 2019
International Pharmaceutical Data Integrity Conference
Feb 2019
Project Management for Non-Project Managers
Feb 2019
Design Verification, Validation and Testing for Medical Devices
Feb 2019
Complaint Handling Best Practices - Compliance with FDA and ISO Regulations
Feb 2019
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
Feb 2019
USP [1224] Transferring the Method to meet Regulatory Expectations
Feb 2019
Understanding FDA Design Verification and Validation Requirements for Medical Devices
Feb 2019
Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products
Feb 2019
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Feb 2019
Complaint Handling, MDR`s & Recalls
Feb 2019
Saudi Sialendoscopy Symposium (SSS)
Jan 2019
OneMedForum San Francisco
Jan 2019
Virtual Seminar on Master Validation Plan - The Unwritten Requirements
Jan 2019
China & Pacific Rim Markets: Compliance Processes for Life Science Products - Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations
Jan 2019
Medical Device Cybersecurity and FDA Compliance
Jan 2019
Tips and Techniques for Handling Missing Data (Statistical Techniques)
Jan 2019
Annual Smart Tech Healthcare
Jan 2019
How to Prepare for an FDA Inspections?
Jan 2019
Controlled Document System for a Life Sciences Manufacturing Plant - Principles of Lean Documents and Lean Configuration
Jan 2019
Understanding Aseptic Technique and Cleanroom Behavior – Avoiding Human Error
Jan 2019
Verification vs. Validation in Regulated Industries
Jan 2019
Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Files , Design Dossiers - The Requirements
Jan 2019
Saudi Health Exhibition & Conference
Jan 2019
International Neuroscience and Biological Psychiatry ISBS Regional (S. America) Conference `NEUROSCIENCE OF STRESS`
Dec 2018
Medicare Iraq Erbil
Dec 2018
Additive Manufacturing Americas
Dec 2018
Boston Medical Affairs Seminar
Dec 2018
Designing an Effective Cleaning Validation for Reusable Medical Devices in Today`s Regulatory Environment
Dec 2018
Validation and Use of Cloud Computing in FDA Regulated Environments
Dec 2018
Intensive Care Society State of the Art Conference (SOA)
Dec 2018
In a Nutshell: Data Protection & Privacy Legislation in the U.S. & European Union
Dec 2018
Annual Healthscape Summit
Dec 2018
TMF Plus and eCTD Plus
Dec 2018
Is your Medical Device Software 510(k) Ready?
Dec 2018
US 3D Technology in Medicine and Healthcare Summit
Dec 2018
HIPAA Privacy Security - Time to Get Serious
Nov 2018
CE Mark Certification: Compile a CE Marking Technical Filecontaining evidence of compliance to the Medical Devices Directive Impact of the MDR for Europe
Nov 2018
International Conference On Biomedical & Health Informatics
Nov 2018
International Conference on Virology, Bacteriology & Infectious Diseases
Nov 2018
Global Pre-Filled Syringes Summit
Nov 2018
Asia-Pacific Conference on Intelligent Medical (APCIM)
Nov 2018
The General Practitioner Conference & Exhibition Melbourne (GPCE)
Nov 2018
Is Your Medical Device Software 510(k) Ready?
Nov 2018
International Conference on Generic Drugs and Biosimilars
Nov 2018
Nordic EUS Conference
Nov 2018
Annual Data, Evidence and Access Summit
Nov 2018
Development of Drug/Device and Device/Drug Combination Products
Nov 2018
Meet the Tougher U.S. FDA CGMPs
Nov 2018
Annual congress on Medicine
Nov 2018
Applied Statistics for Scientists and Engineers
Nov 2018
Astana Zdorovie
Nov 2018
Keeping Up-To-Date as a (GMP) Qualified Person
Oct 2018
The A to Z`s of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems for Bio-pharma, Medical Devices and Cosmetics Industries
Oct 2018
HPAPI World Congress
Oct 2018
Japan: Regulatory Compliance Requirements for Life Science Products
Oct 2018
The Next Level of Private Practice - Risk, Referrals, Retention & Resilience
Oct 2018
Uncovering and Managing Successful Post Market Compliance for Medical Devices
Oct 2018
Advanced Imaging Update
Oct 2018
International Conference on Robotics and Automation
Oct 2018
Requirements for IQ, OQ and PQ Quality Protocols
Oct 2018
Combination Products
Oct 2018
HR Life Sciences
Oct 2018
Metrology: Statistical Analysis of Measurement Uncertainty
Oct 2018
Combination Products
Oct 2018
Strategies for Improving Effectiveness and Efficiency of your Quality Management System
Oct 2018
Advanced Heart Failure Summit: Anniversary Celebration of Ventricular Assist Device and Heart Transplantation (AHF)
Oct 2018
Change Control Procedures in Regulated Industries
Oct 2018
Good Documentation Guideline (Chapter 1029 USP)
Oct 2018
Aseptic Process Overview and Validation
Oct 2018
Advanced Search Webinars EU Medical Device Regulation (MDR) - Updated CE Marking Process & ISO 13485:2016 Expectations
Oct 2018
International Conference on Medical Innovations
Oct 2018
Annual Biomarkers - CDx - Precision Immunotherapy Summit
Oct 2018
Annual Microbiome: Translating into Diagnostics and Therapeutics Summit
Oct 2018
Medical Device Technology Exchange (MDTX)
Oct 2018
Powerful Closed-loop CAPA - Meeting FDA Expectations
Oct 2018
FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Oct 2018
China International Healthcare & Recovery and Gerontic Products Expo
Sep 2018
How FDA Trains Its Investigators and Inspectors to Review Sub-Systems for State of Compliance: What You Need to Do to Prepare for a Successful Inspection
Sep 2018
Tougher Supplier Controls – Avoid Unwanted Changes
Sep 2018
Software Risk Management
Sep 2018
Auditing and Qualifying Suppliers and Vendors
Sep 2018
Marketing & CX in the Pharmaceutical Industry
Sep 2018
Inhalation and Respiratory Drug Products Conference
Sep 2018
FDA`s New Enforcement of 21 CFR Part 11
Sep 2018
Successful Computer System Validating and Control Using Managed Services SaaS, and Cloud Based Platforms
Sep 2018
Writing Effective Analytical Procedures
Sep 2018
International Colloquium on Medical & Clinical Trials
Sep 2018
Hosting FDA Regulatory Inspections
Sep 2018
Statistics for Process and Quality Control
Sep 2018
Medicinal Chemistry Summit: USA
Sep 2018
Gut Health Congress Asia
Sep 2018
International Conference on Hepatobiliary & Pancreatic Disorders
Sep 2018
Annual Clinical Trials Quality & Compliance
Sep 2018
Quality Agreements Made Easy
Sep 2018
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
Sep 2018
Compliance for Risk Based Approaches for Clinical Trials
Sep 2018
Chipping away at constraints – Practical tips to Improve your Manufacturing Operations
Sep 2018
Medical Device Cybersecurity -Improving Compliance and your Company`s Bottom Line
Sep 2018
Medical Fluid Bags
Sep 2018
Laboratory Controls – Anticipate the Systems Based FDA Inspection
Sep 2018
Medical Tubing
Sep 2018
Life Science Knowledge Management Summit
Aug 2018
International Conference on World HPLC & Separation Techniques
Aug 2018
Marketing to Medicare or Medicaid Beneficiaries - What You Can and Cannot Do
Aug 2018
Medical Device Value Engineering
Aug 2018
Purchasing Controls for Medical Devices
Aug 2018
What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections
Aug 2018
Global Experts Meeting on Clinical Research and Clinical Trials
Aug 2018
Design Control Basics
Aug 2018
Deciding When to Submit a 510(k) for a Change to an Existing Device
Aug 2018
Building a Compliant Documentation and Training System
Aug 2018
FDA Compliant QC and QA Practices – Creating a Perfect, Audit-Ready QMS
Aug 2018
Quality by Design for Medical Devices – Essential Techniques
Aug 2018
International Conference on Telemedicine & Medical Informatics
Jul 2018
Statistical Analysis for Product Development
Jul 2018
Laboratory Investigations for Out of Specification Results
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
International Conference on Cancer Therapy
Jul 2018
Annual Conference on Clinical Research & Biomarkers
Jul 2018
Onboarding In A GMP Environment – Best Practices
Jul 2018
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Jul 2018
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay that Way
Jul 2018
The International Search & Rescue Conferences & Exhibition
Jul 2018
Deviation Investigation Best Practices: Ensuring Correct Content and Conclusions
Jul 2018
Patients Suing Under HIPAA
Jul 2018
Project Management for FDA-Regulated Companies
Jul 2018
Additive Manufacturing Europe
Jun 2018
Ligature Risks: Ensuring Compliance with the CMS Hospital CoPs and TJC Requirements
Jun 2018
510(k) Documentation Best Practices for Software or Software Enabled Medical Devices
Jun 2018
Biocompatibility Testing; what you need to know
Jun 2018
Food Fraud in the Organic Industry
Jun 2018
Overview of Medical Device Regulation in Europe
Jun 2018
Electrocardiography For Practititioners, An Interactive Course for Clinicians
Jun 2018
37 C Life Science Technology & Business Conference & Exhibition
Jun 2018
Things you need to know about information governance to sell healthtech products into the NHS
Jun 2018
PharmaCon Expo
Jun 2018
International Symposium for Molecular Medicine
Jun 2018
Oversight of CROs-Vendors-CMOs
Jun 2018
World Pharmacists & Clinical Pharmacy Annual Congress
May 2018
Effective Complaint Handling, Medical Device Reporting and Recalls
May 2018
Pharmaceutical Logistics
May 2018
Why and How - Verification of Compendial Methods - USP [1226]
May 2018
World Liver Conference
May 2018
Gaining and Re-Establishing Control of Your Cleanroom
May 2018
Off-Label Regulatory Compliance Congress
May 2018
Product Recalls Forum
May 2018
Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations
May 2018
Document Control and Change Control Process in GxP/GMP Environment
May 2018
NANO.IL. - The International Nanotechnology Conference in Israel
May 2018
Root Cause Analysis: Foundation of Investigations and CAPA
May 2018
Mobile in Clinical Trials Europe
May 2018
GMP Expectations for Products Used in Early Phase IND Studies
May 2018
Health Product Marketing authorization in Brazil - Documentation, Approval Process, Labeling, Advertising and Post Market Vigilance
May 2018
Vietnam Medi-Pharm
May 2018
Different requirements for Phase I Investigational Drug Products:
May 2018
CHI`s Clinical Trial Oversight Summit
May 2018
Global Cyber Security in Healthcare & Pharma Summit
May 2018
Fundamentals of Risk Management in Clinical Research
May 2018
How to Comply with 21 CFR 11 Requirements for Electronic Medical Records
May 2018
Managing Your FDA Inspection: Before, During and After
Apr 2018
Serialisation And Tracking Of Pharmaceutical Products Summit
Apr 2018
Edition Nordic Market Access Leaders Forum
Apr 2018
Preparing the Marketing Authorization Application in the EU, with a focus on the product information
Apr 2018
mHealth for Clinical Trials EU
Apr 2018
The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities
Apr 2018
MED-e-TEL
Apr 2018
Annual Peter D. Stevens Course on Innovations in Digestive Care
Apr 2018
Kuwait Medica Conference & Exhibition
Apr 2018
Asthma and COPD
Apr 2018
International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems
Apr 2018
eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Apr 2018
A Risk Based Strategy for the Development & Validation of and Validation of Analytical Methods with a QbD Approach
Apr 2018
Evolution of the Quality Management System - How to go from Surviving to Thriving
Apr 2018
Medical Device Single Audit Program (MDSAP) Preparation
Apr 2018
Software Validation for the New FDA Inspections
Apr 2018
Central Labs & Diagnostics Partnerships Forum
Mar 2018
Congress of Musculoskeletal Imaging at Bajio,
Mar 2018
The DHF, Technical File and Design Dossier - Similarities, Differences and the Future
Mar 2018
Medical Devices Summit
Mar 2018
LabtechMED Eurasia
Mar 2018
Central Monitoring Summit
Mar 2018
Pre-Filled Syringes
Mar 2018
TMF Operations: a Quality and Regulatory Approach
Mar 2018
annual Conference on Pediatric Clinical Trials
Mar 2018
A Risk Based Approach To IT Infrastructure Qualification & Compliance
Mar 2018
Global CDx & Personalized Medicine Summit
Mar 2018
Analytical Method Validation
Mar 2018
Essentials of Dealing with Non-Conforming Material
Mar 2018
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program
Mar 2018
Ensuring Data Integrity in Method Validations
Feb 2018
Bioavailability and Bioequivalence Studies Submitted in NDAs and INDs for Orally-Administered Drug Products
Feb 2018
GMP for Quality Control Laboratories and FDA Audit Preparation
Feb 2018
A Risk Based Approach To Data Integrity
Feb 2018
Acceptance Activities in FDA QSR
Feb 2018
Management Control - Underutilized and Underappreciated
Feb 2018
The New ISO 13485:2016 and Comparison with 21CFR820 - How to Comply with both in the Same Organization
Feb 2018
Unique Device Identification (UDI) - GUDID: Final Rules, Implementation and Compliance
Feb 2018
Medical Imaging in Clinical Research
Feb 2018
Risk Management in Clinical Trials
Feb 2018
Cardiac Arrhythmias: Mysteries of Electrophysiology Unraveled
Feb 2018
Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans
Feb 2018
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Feb 2018
Medlab ME
Feb 2018
Good Manufacturing Practices for Active Pharmaceutical Ingredients per ICH Q7
Feb 2018
Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigation
Feb 2018
Validation of FDA-Regulated Computer Systems
Feb 2018
Quality Audits for the Medical Device Industry
Jan 2018
HTC-15 - International Symposium on Hyphenated Techniques in Chromatography and Separation Technology
Jan 2018
Verification vs. Validation - Product Process Software and QMS
Jan 2018
A Risk Based Approach to Testing of Computerized GxP Systems
Jan 2018
Medical Device Software An Incremental Approach to Risk and Quality Management
Jan 2018
FDA`s Software Monsters: Cybersecurity, Interoperability, Mobile Apps and Home Use
Jan 2018
Onsite GCP Review and Update including the all-important `Investigators Responsibility
Jan 2018
Innovation & mHealth in Clinical Trials
Jan 2018
Risk Based Project Management for the Life Sciences Industry
Jan 2018
Trial Master File for Clinical Data Systems Regulated by FDA
Jan 2018
The Value of a Human Factors Program
Jan 2018
Validation and 21 CFR Part 11 Compliance of Computer Systemst
Jan 2018
21 CFR Part 11 Compliance - Ensuring Data Integrity and Safety in Clinical Research
Jan 2018
Kenya Tradex
Dec 2017
International Conference on Healthcare and Biological Research (ICHBR)
Dec 2017
Med- tech Summit
Dec 2017
Excel Spreadsheets - Step-By-Step Instructions for Compliance
Dec 2017
Why you Should be Worried about HIPAA
Dec 2017
Design History Files, Device Master Records and Quality Management System for Medical Device Company - Principles of Lean Documents and Lean Configuration
Dec 2017
Integration of ERP and Legacy FDA-Regulated Systems
Dec 2017
Why are we Seeing More Independent Data Safety Monitoring
Dec 2017
robocare: a multidisciplinary view of practical and ethical issues
Dec 2017
Healthcare CyberSecurity Summit
Nov 2017
Annual COPD: Novel Therapeutics and Management Strategies
Nov 2017
Human Subjects Research Seminar: Current Regulations under FDA and HIPAA
Nov 2017
The GIANT Health Event
Nov 2017
Dealing with Performance Issues
Nov 2017
Lab Automation & Robotics
Nov 2017
Life Science IP
Nov 2017
International Conference and Exhibition on Pharmaceutical Science and Pharmacognosy
Nov 2017
Design of Experiments and Statistical Process Control for Process Development and Validation
Nov 2017
Digital Pathology Congress
Nov 2017
EAI International Conference on Wireless Mobile Communication and Healthcare
Nov 2017
international conference on digital pathology and image analysis
Nov 2017
Women in Pharma and Medical Leadership Summit
Nov 2017
GMP and Regulatory Expectations for Early IND Products
Nov 2017
FDA`s Latest Regulations for Tobacco Industry Effective 8-2016
Nov 2017
AAMI TIR 45: Agile Meets Software Standards, and we all Win
Nov 2017
The World Congress of Biomedical Engineering (WCBME-)
Nov 2017
Global Nursing and Healthcare Summit
Nov 2017
Statistics for the Non-Statistician
Nov 2017
Statistical Methods A Visual Approach
Nov 2017
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Nov 2017
World Congress and Exhibition on Vaccines, Vaccination and Immunization
Nov 2017
MedTech Commercial Leaders Forum USA
Nov 2017
Medical Device Hazard Analysis Following ISO 14971
Nov 2017
Annual Summit on Nanomedicine & Its Applications
Nov 2017
The Future of Supply Chain - 7 Megatrends that will Transform the Global Marketplace
Nov 2017
Global Clinical Connect
Nov 2017
Annual Adaptive Design Clinical Trials Summit
Nov 2017
Virtual Seminar on Analytical Method Validation Process
Nov 2017
World Clinical Medicine & Collaboration Forums
Oct 2017
Annual Clinical Forum and Exhibition
Oct 2017
Annual Partnerships in Clinical Trials US
Oct 2017
Dubai Thrombosis
Oct 2017
Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach
Oct 2017
Annual Companion Diagnostics (CDx) Summit Oncology & Beyond: Clinical Applications, Regulation, & Reimbursement
Oct 2017
Laboratory Instrument Qualification
Oct 2017
Validation, Verification and Transfer of Analytical Methods from FDA/EMA, USP and ICH
Oct 2017
Managing Your FDA '483' Inspectional Observations
Oct 2017
Medical Technology
Oct 2017
DMC Optimization Summit
Oct 2017
ICEIAM : International Conference on Environmental, Industrial and Applied Microbiology
Oct 2017
International Conference on Clinical and Medical Case Reports
Oct 2017
Developing the Risk Management File
Oct 2017
Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices
Oct 2017
International Conference on Biomedical Engineering (ICBE)
Oct 2017
Medical Device Engineering Change Control
Oct 2017
Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval
Oct 2017
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes
Oct 2017
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2017
Computer System Validation - Reduce Costs and Avoid 483s
Oct 2017
Digital Marketing Innovation Summit in Healthcare Industry
Oct 2017
Standards for Medical Device Software: Friend, not Foe
Oct 2017
Design Controls for Medical Devices - Regulations, Myths, Challenges, and Best Practices
Oct 2017
Excellence in Pharmacovigilance: Clinical Trials and Post-Marketing
Oct 2017
MEDTEC Ireland
Oct 2017
Pricing & Reimbursement Conference
Sep 2017
NCCR - National Conference for Clinical Research
Sep 2017
Annual Pre-Filled Syringes Summit
Sep 2017
Design of Experiments (DOE) for Process Development and Validation
Sep 2017
FierceBiotech Drug Development Forum
Sep 2017
ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices
Sep 2017
International Conference and Expo on Heart Surgery
Sep 2017
Annual Cancer Immunotherapy Summit
Sep 2017
Effective Training Practices for FDA Compliance
Sep 2017
Artificial Intelligence Innovation Summit
Sep 2017
VSICON
Sep 2017
Supplier Management in FDA- and ISO-regulated Industry
Sep 2017
Best Practices for an Effective Cleaning Validation Procedures
Sep 2017
Modern Vaccines Adjuvants and Delivery Systems (MVADS)
Sep 2017
Life Science Investor Relations Forum
Sep 2017
Production and Process Control: Building a Robust System
Sep 2017
Medical Equipment Fair - China International Wisdom Medical & Wearable Device Expo
Sep 2017
Annual Medical Affairs Leaders Forum Asia
Aug 2017
Commercialization of Micro, Nano, and Emerging Technologies (COMS)
Aug 2017
Acceptance Sampling - Methods and Applications
Aug 2017
European Regulatory Procedures - Comprehensive Overview of EMA and National Requirements and other Agencies
Aug 2017
HIPAA Under Trump - What to expect and How to comply
Aug 2017
FDA`s Medical Device Clinical Trials Program
Aug 2017
Excel Workbooks and FDA Device Regulations
Aug 2017
Device Accessories - Understanding and Implementing the Final Guidance Document
Aug 2017
Medical Device Hazard Analysis Following ISO
Aug 2017
Documenting Software for FDA Submissions
Aug 2017
Laboratory-Developed Tests: Why does FDA think they can Regulate them, and why do others think they Cannot
Aug 2017
FDA Regulations for Environmental Monitoring (EM) Program
Aug 2017
How to Prepare for and Host a FDA Inspection and Respond to 483`s
Aug 2017
FDA Legal Writing Skills that Result in Effective Regulatory & Quality Submissions
Aug 2017
Rare Disease Collaboration Summit
Jul 2017
International Endoscopy Conference
Jul 2017
Understanding Aseptic Technique and Cleanroom Behavior
Jul 2017
Post-Compliance Medical Device Regulations and Evolving Reporting Requirements: Complaint Handling, Medical Device Reporting/ eMDR and Recalls and their compliance with UDI`s
Jul 2017
World CDx: Market Access for Precision Medicine
Jul 2017
Trial Protocol Optimization and Design Congress
Jul 2017
Personnel Training to Assure FDA and ISO Compliance
Jul 2017
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies
Jul 2017
Understanding the FDA`s Regulation of HCT/Ps and Successful Product Development Strategies
Jul 2017
Senior Expo Asia
Jul 2017
Statistical Concepts of Process Validation
Jul 2017
Canadian Pharma Market Research Conference
Jun 2017
Proton Therapy USA
Jun 2017
Writing Effective Standard Operating Procedures and Work Instructions
Jun 2017
How To Establish an Effective Chief Compliance Officer`s (CCO) or Chief Risk Officer`s (CRO) Function - Organization and Responsibilities
Jun 2017
Overview of Device Regulation - FDA
Jun 2017
Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines
Jun 2017
Wound Care: From Innovations to Clinical Trials
Jun 2017
Annual European Spare Parts Management Summit
Jun 2017
Medical Device - Engineering Change Control
Jun 2017
Cleaning Validations Using Extraction Techniques
Jun 2017
Good Clinical Practices (GCP) - Understanding and Implementing the Current Global Requirements
Jun 2017
The New Clinical Trials Regulation and Regulatory Affairs Aspects of Medicinal Product Development in the EU
Jun 2017
Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines
Jun 2017
In-Vitro Diagnostics
Jun 2017
International Summit on Vaccines Business & Immunology (Innovate Immunology)
Jun 2017
Packaging for Parenterals Summit
Jun 2017
AMI`s Medical Tubing
Jun 2017
FDA Policy and Goals Regarding the 483 Response
Jun 2017
Healthcare Medical Software/Applications - Risks, Validation & Interoperability
Jun 2017
Traceability and the Drug Quality and Security Act Conference
May 2017
Auditing for Medical Device and Pharma Companies – A Tool to Reduce Quality and Compliance Risk
May 2017
Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)
May 2017
Radiation Sterilization of Medical Products - Beyond the Basics
May 2017
FDA’s 21 CFR Part 11 Add-on Inspections
May 2017
Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data
May 2017
Efficient Process Validation Strategies and Validation Master Plan (VMPs) for Medical Devices
May 2017
Data Integrity: FDA/EMA/TGA Requirements and Implementation
May 2017
Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
May 2017
Medical Device Employee Training -Requirements and Implementation tips
May 2017
Medical Device Reporting Requirements for Manufacturers Final Guidance
May 2017
FDA Scrutiny of Promotion and Advertising Practices
May 2017
How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare
May 2017
FDA`s GMP Expectations for Phase I and -in-Man Clinical Trials
May 2017
Human Factors and Predicate Combination Products
May 2017
Extractables & Leachables USA
May 2017
Introduction to the Medical Device Directives
May 2017
Implementing MDSAP (Medical Device Single Audit Program) for Compliance Success
May 2017
Laboratory, Medical and Device Performance and Validation following Regulatory
May 2017
IPhEB & CPhi Russia
Apr 2017
Healthcare Asia Pacific Summit
Apr 2017
MSL Society ONBOARD TRAINING PROGRAM
Apr 2017
Best Practices for Preparation for, Behavior during, and Response to an FDA Inspection
Apr 2017
Medical Records: Responding to Subpoenas and Investigations
Apr 2017
Apteka Expo
Apr 2017
GxP (GMP, GLP, GDP) Data Integrity, Quality Metrics and FDA Inspections
Apr 2017
Medical Device Recalls: a Preventive Strategy
Apr 2017
Computer Systems Validation (CSV), Data Integrity, 21 CFR Part 11 Compliance and GAMP 5
Apr 2017
PMBA - Project Management Business Administration
Apr 2017
Spring International Conference on Biomedical Engineering and Biotechnology (BEB-S)
Apr 2017
Effective Purchasing and Supplier Controls for Medical Device Manufacturers
Apr 2017
Efficient and Effective FDA and ISO Management Reviews
Apr 2017
Packaging and Labelling for Clinical Products
Apr 2017
Quality by Design - Essential Techniques for Medical Devices
Apr 2017
Medical Device Premarket and Post market Cyber security following the new FDA Guidances
Apr 2017
Preparing a US FDA Medical Device 510(k) Submission and Deciding When to Submit a 510(k) for a Change to an Existing Device
Apr 2017
SudTec
Apr 2017
MDTI - Medical Device School
Apr 2017
Medical Necessity: Can you define it, Capture it, Document it
Apr 2017
Insight into Requirements of PMDA for Marketing Medical Products in Japan
Mar 2017
analytica Vietnam
Mar 2017
Pharmaceutical Sciences 17 / International Conference on Pharmaceutical Sciences
Mar 2017
Data Analysis in QSR
Mar 2017
Classifying Medical Devices - US and EU
Mar 2017
Pre-Filled Syringes
Mar 2017
The International Conference on Minimally Invasive Medicine (MIM)
Mar 2017
FDA & CFIA 2016 Regulatory Changes/Updates
Mar 2017
21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration
Mar 2017
PTI - Clinical Research Project Management
Mar 2017
Quality Audits for the Medical Device Industry
Mar 2017
Global Precision Medicine Summit
Mar 2017
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration
Feb 2017
Powers of Attorney: Medical Records Release Concerns
Feb 2017
Annual Data and Technology in Clinical Trials USA
Feb 2017
Clinical Trial Monitoring: A Sponsor Responsibility
Feb 2017
Latin America Regulatory Compliance: Current Challenges in Argentina, Brazil and Mexico
Feb 2017
Understanding Design Controls
Feb 2017
Three-dimensional cell culture: Innovations in tissue scaffolds and biomimetic systems
Feb 2017
Spotlight on Post Market Surveillance
Feb 2017
Microsoft Excel Series - Part 2: Learn More about Macros
Feb 2017
How to conduct a Human Factors and Usability validation following ISO62366 and the new FDA Guidance
Feb 2017
Annual Conference and Exhibition for the Medical Device Design & Manufacturing Industry (MDDMI)
Feb 2017
Techniques for Medical Device Packaging
Feb 2017
Disaster Recovery (DR) and Business Continuity Planning (BCP) Best Practices for an FDA-Regulated Environment Increasingly Challenged by Cyber Attacks and Other Threats
Jan 2017
Requirements for Registration of Medical Device Products in China
Jan 2017
The Sunshine Act: Reporting for Clinical Trials
Jan 2017
Microsoft Excel Series - Part 1: Shake Hands with Macros
Jan 2017
Chemistry 101 for Medical Device Regulatory & Quality Professionals: Essential knowledge needed to Manage Drug&Device Combination Product Project
Jan 2017
FDA Regulation of Combination Products
Jan 2017
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Jan 2017
Implementation of Risk Evaluation and Mitigation Strategy (REMS) Programs in a Health System
Jan 2017
digital healthcare innovation series: internet of things, wearables, sensors, assistive devices
Jan 2017
HIPAA Breach Notification Rule - What you must do to Comply
Jan 2017
The New FDA-Product Approval, Inspection, and Enforcement
Jan 2017
Fundamentals of the de novo process for medical devices: What you need to know when pursuing a de novo application and approval with the FDA
Jan 2017
Effective Corrective and Preventive Action Program (CAPA): The Role of Corrective Action and Preventative Action in Your Quality Management System
Jan 2017
Opal Medical Device Summit
Jan 2017
Navigating the New European Clinical Trial Regulation (EUCT Regulation 536-2014)
Jan 2017
Corrective and Preventive Action (CAPA)
Jan 2017
Adverse Event Management During Medical Device Clinical Studies
Jan 2017
How to Handle HIPAA Security Incidents Breaches, Complaints, and Investigations
Dec 2016
Quality and Compliance - Building Your Key Capabilities for Future Success
Dec 2016
Clinical Evaluation Reports (CER`s) Required for All Medical Devices in Europe
Dec 2016
CDRH/Payer Summit for Medical Device Executives
Dec 2016
Hands-On Abdominal Ultrasound Imaging & Doppler Course
Dec 2016
Statistical Methods for Design Verification, Process Validation, and Process Control
Dec 2016
Best Practices for FDA Inspection
Dec 2016
Device Master Record - Can DMR show the way to comply with QSR?
Dec 2016
International Conference on Precision Medicine
Dec 2016
Product Risk Management Under ISO 14971:2007 and ICH Q9
Dec 2016
Introduction to Bedside Ultrasound Course for Intensivists, Emergency Room Staff, and New Technologists
Dec 2016
BIOMEDevice San Jose
Dec 2016
Capsule Based Inhalers: Understanding the Science
Nov 2016
European Medical Device Regulation Workshop: Change Management
Nov 2016
How to Manage a Medical Device Recall Efficiently and Effectively
Nov 2016
International Conference on Medicine and Medical Education (ICMME)
Nov 2016
Telemedicine & eHealth
Nov 2016
SANS Healthcare Cyber Security Summit & Training
Nov 2016
Validating Radiation Sterilization for Medical Products
Nov 2016
International Conference on Scientific and Medical Writing
Nov 2016
International Conference on Endoscopy
Nov 2016
International Conference on Chest
Nov 2016
Medical Devices - ISO 13485 - Do you really know what you need to?
Nov 2016
510(k) Preparation with New Released FDA Guidance on Product Modifications
Nov 2016
IP Life Sciences Exchange
Nov 2016
Effective Complaint Handling & Medical Device Reporting
Nov 2016
International Conference on Biomedical Engineering and Science (BES)
Nov 2016
CGMP Quality Principles for the FDA Regulated Industries: 2-Day In-Person Seminar
Nov 2016
Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
Nov 2016
In Vitro Diagnostics: Oncology and Infectious Diseases Conference
Nov 2016
Preparing for the Upcoming EU Medical Device Regulations
Nov 2016
Singapore International ROBO Expo
Nov 2016
HIPAA Security & Privacy Risk Analysis- OCR Audits
Oct 2016
Biologics World China
Oct 2016
Hands-On Tactile Breast Ultrasound Imaging & Doppler Course
Oct 2016
Software Design for Medical Devices Summit (SDMD)
Oct 2016
Hands-On Obstetric & Pelvic Ultrasound Imaging and Doppler Course
Oct 2016
Laboratory Instrument Calibration: Current FDA Regulatory Requirements and Best Practices
Oct 2016
Why is FDA at my facility, and what do I do during an inspection?
Oct 2016
Fundamental Laboratory Record Keeping and Compliance Issue
Oct 2016
Developing Documents and Records to meet the Requirement of ISO 17025
Oct 2016
FDA Inspection: Do`s and Don`ts
Oct 2016
Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes
Oct 2016
International Forum Healthcare Management (HCM)
Oct 2016
Design and Execution of Stability Studies for Biologics
Oct 2016
Auditing Clinical Trials for Good Clinical Practice (GCP) Compliance
Oct 2016
Clinical Trial Audits in Practice
Oct 2016
MATERIALS` (Ottawa, CANADA:)
Oct 2016
Test Methods and Standards for Medical Device Design Verification and Validation
Oct 2016
Diagnostics Summit
Oct 2016
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2016
MEDDEV 2.7.1, Revision 4 for Clinical Evaluation and the Latest Guideline: A Guide for Manufacturers and Notified Bodies
Oct 2016
Learning Design Controls through Review of FDA 483 Observations
Oct 2016
Data Integrity: FDA/EU Requirements and Implementation
Oct 2016
3 Day Masterclass - Clinical Trials
Oct 2016
Artificial Intelligence in Health & Life Sciences Conference
Oct 2016
HIPAA Training for the Compliance Officer
Oct 2016
Asia-Pac Trial Master File Summit
Oct 2016
Production and Process Control: Building a Robust System for Medical Device Companies
Oct 2016
Technical Writing for Medical Products: SOPs, Investigations and Change Records
Sep 2016
International Rehabilitation Shanghai Forum
Sep 2016
Ensure Your Healthcare Compliance Program Reaches Optimal Potential and Protect your Organization
Sep 2016
Clinical Trial Management Essentials
Sep 2016
Setting and Measuring Quality Objectives
Sep 2016
Medical Record Standards: What Hospitals Should Know About the CMS Hospital CoPs
Sep 2016
Supplier Management for Medical Device Manufacturers
Sep 2016
How to prepare for and Host FDA Inspection and Avoid 483`s
Sep 2016
Medical Device Tracking: Latest FDA Update and Expectations
Sep 2016
The European Microscopy Congress (EMC)
Sep 2016
Handling, Storage, Distribution, and Installation of Medical Devices
Sep 2016
FDA Regulation of Digital Health - Current Status and Recent Developments
Aug 2016
Business Continuity or Disaster Recovery Planning
Aug 2016
How FDA Trains Its Investigators to Review Sub-Systems for State of Compliance: What You Need to Do to Prepare for a Successful Inspection
Aug 2016
EHS Incident Prevention - Proactive EHS Programs
Aug 2016
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)
Aug 2016
Global Medical Device Regulation
Aug 2016
OIG Work Plans: How They Impact Providers
Aug 2016
Risk Based Approach for Medical Device Design Control
Aug 2016
Chiropractic & ICD-10
Aug 2016
Clinical Trials be at Risk for Potential Fraudulent Billing. Conducting a Billing Risk Assessment and Coverage Analysis are Essential for Proper Billing.
Aug 2016
Changes to the Common Rule (45 CFR 46) : What this means for you
Aug 2016
Tougher Import Rules for FDA Imports in
Aug 2016
How to do a Risk Analysis
Aug 2016
How to Prepare for Increased HIPAA Enforcement
Aug 2016
Creating Reader-Focused Technical Documents in FDA Regulated Industries
Aug 2016
FDA Scrutiny of Purchasing/Supplier Controls
Aug 2016
EMBL Conference: Microfluidics
Jul 2016
Complaint Handling and Management: From Receipt to Trending
Jul 2016
Marketing Products without Getting Hammered by FDA
Jul 2016
Why is FDA at my facility, and what do I do during an inspection?
Jul 2016
Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada
Jul 2016
FDA`s Emerging Signals Guidance: Reporting Medical Device Safety Warnings
Jul 2016
FDA Issues Draft Guidance for 3D Printed Medical Devices
Jul 2016
Using Analysis of Variance (ANOVA) - A Practical Approach
Jul 2016
Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Water Systems for Bio/Pharma, Medical Devices, and Cosmetics Industries
Jul 2016
Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
Jul 2016
Standards and Their Role in Medical Device and Patient Safety
Jul 2016
Human Factors/Usability Based on ISO 62366
Jul 2016
FDA QSR Training (21 CFR Part 820) for Medical Device Companies
Jul 2016
Life Sciences Risk Management A to Z - Best Practices for Effectiveness and Efficiency: 2-Day Workshop
Jul 2016
Good Documentation Practices (GDP)
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
PFS-Tech
Jun 2016
Polymers & Plastics in Medical Devices
Jun 2016
BioLogistics Summit
Jun 2016
National Neurotrauma Symposium
Jun 2016
Technical Writing for the Pharmaceutical, Medical Device and Biotech Industries
Jun 2016
Balkan & National Congress of Nuclear Medicine, BCNM
Jun 2016
Understanding and Implementing the Medical Device Directive: 2-Day In-person Seminar
Jun 2016
Mouse Models: Genetics Breeding and Experimental Design
Jun 2016
Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
Jun 2016
FDA`s Low-Risk Device Policy and the Impact on Mobile Medical Device Applications
Jun 2016
Clinical Trial Regulatory Guideline Requirements
Jun 2016
Verification vs. Validation - Product Process Software and QMS
Jun 2016
Pharma, Pricing & Marketing Access
Jun 2016
Analytical Method Validation under Good Laboratory Practices (GLPs)
Jun 2016
International Biopharmaceutical R&D Innovation New Asia Summit
May 2016
Marketing Products Without Getting Hammered by FDA
May 2016
Supplier Management for Medical Device Manufacturers
May 2016
Complying With Telemedicine Requirements
May 2016
FT Asia Healthcare and Life Sciences Summit
May 2016
Biennial Australian Association for the Manual Handling of People Conference
May 2016
PLM Road Map for the High Tech & Medical Device Industries
May 2016
Adverse Event Reporting: Site and Sponsor Reporting Requirements for Investigational Products
May 2016
Internal Auditing for the Medical Device Industry
May 2016
Edition Healthscape Summit
May 2016
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)
May 2016
An Ethical Use of Electronics, EHR, and e-Anything
May 2016
GMP Complaint Systems and Product Recalls
May 2016
Implementing Validation and Qualification - Annex 15 and FDA Requirements
May 2016
Validation of a HPLC/UPLC Methodology
May 2016
Risk Management for Medical Devices
Apr 2016
The Data Clinic – Sydney
Apr 2016
Best Practices for Compliance with FDA 21CFR1040
Apr 2016
Integration of Human Factors into Medical Device Design: FDA and European Commission
Apr 2016
Data Quality and Technology in Clinical Trials
Apr 2016
The Importance of the Investigator Responsibilities and Legal Commitments in Drug and Device Clinical Research in Achieving a Clean Audit
Apr 2016
Iraq Health Expo
Apr 2016
The China （Beijing）Medical Equipment Expo
Apr 2016
Packaging and Labeling for Commercial and Clinical Products
Apr 2016
Electronics New England
Apr 2016
LABOTEC
Apr 2016
NextMed / MMVR22 (Medicine Meets Virtual Reality)
Apr 2016
FDA Import, Export and Foreign Operations for Medical Devices and Pharmaceuticals
Apr 2016
Medical Coding, Billing and Documentation
Apr 2016
How Fixing FDA Compliance Problems (Remediation) Aligns with the 5 Stages of Grief
Apr 2016
Integration of ERP and Legacy FDA-Regulated Systems
Apr 2016
Evaluating the Effectiveness of a Corporate Compliance Program
Mar 2016
Process Validation for Medical Devices: 2-day In-person Seminar
Mar 2016
Medical Device Asia Pacific Summit
Mar 2016
Device Changes and the 510(k)
Mar 2016
Fraud and Abuse in the Sales & Marketing of Medical Devices
Mar 2016
Writing and Enforcing Effective SOPs
Feb 2016
Investing in Medical Innovations – Congress & Fair (IMICF)
Feb 2016
Root Cause Analysis - The Heart of a Successful CAPA Program
Feb 2016
IMDI
Feb 2016
Designing and Monitoring Approvable Medical Device (cardiovascular) Protocols
Feb 2016
Global Nursing Management Conference
Feb 2016
Mastering the HIPAA Privacy, Security, and Breach Notification Rules: Coping with Rule Changes, Managing Incidents, Preparing for Audits, and Avoiding Penalties
Feb 2016
HIPAA Upcoming Changes
Jan 2016
Medical Device Complaint Handling
Jan 2016
Creating Effective SOP for Regulatory Compliance
Jan 2016
Medicare Penalties and Incentives – Update for Medical Practices
Jan 2016
Medical Devices Designing with Cleanliness in Mind
Jan 2016
Managing FDA Inspections from Readiness through Follow Up Responses
Jan 2016
How to Develop a Master Validation Plan
Jan 2016
Investigational Device Accountability
Jan 2016
Good Laboratory Practice Compliance Monitoring Summit
Jan 2016
Compliant Clinical Research Conduct: What Every Clinical Research Professional Needs to Know
Jan 2016
Navigating Ethics and Law for Mental Health Professionals: Ethical practice; Risk management, and; Professional codes of ethics
Jan 2016
Toyota Kata - Wax On, Wax Off (in partnership with ASQ Lean Enterprise Division)
Jan 2016
Complaint Handling & Medical Device Reporting (MDR)
Jan 2016
FDA`s Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List
Jan 2016
FDA`s New Enforcement of 21 CFR Part 11
Jan 2016
FDA Inspection Lessons Learned: Lack of Trial Oversight
Jan 2016
How to Respond to an FDA Investigation: What happens when the FDA threatens to shut you?
Jan 2016
Quantitative Benefit-Risk Assessment for the New PSUR
Dec 2015
Basics of US Medical Device Regulation
Dec 2015
RoboUniverse San Diego
Dec 2015
Surviving an FDA Inspection: Understand the Do`s and Don`ts and the Ground Rules
Dec 2015
Registration & Listing, FDA Inspection Strategies and Compliance Initiatives - Medical Device
Dec 2015
HIPAA - Portable Devices and Enforcement
Dec 2015
Kenya Medex
Dec 2015
Equipment, Facility, and Process Qualification and Validation - A Simple Top to Bottom Sustainable Approach
Dec 2015
The Most Common Coding Errors and How to Avoid them
Dec 2015
Corrective and Preventive Action (CAPA) and Complaint Handling in Medical Device.
Dec 2015
Developing a Validation Master Plan
Dec 2015
Objectionable Microorganisms: Considering the Risk
Dec 2015
Digital Hospital of the Future, Australia
Nov 2015
Effective Strategy for Medical Device Recalls
Nov 2015
Medical Design & Manufacturing (MD&M Florida)
Nov 2015
Life Science Competition Congress
Nov 2015
Regulatory Crisis Management: Best Practices for Dealing with the Common Crisis Events for the FDA-Regulated Industry
Nov 2015
An Introduction to the Medical Devices Directive
Nov 2015
ICH-FDA Good Clinical Practice – Managing Clinical Trials
Nov 2015
Medical Design & Manufacturing (MD&M) Chicago
Nov 2015
Advanced Manufacturing Meetings Baja California
Nov 2015
MEDEVAC
Oct 2015
The Pharmaceutical and Medical Device Labelling Summit
Oct 2015
Clinical Trials Workshop
Oct 2015
Development regulatory affairs for Oncology Medicinal Products
Oct 2015
How to Prepare for, Manage, and Follow-up to an FDA Inspection: Risk-driven Approach
Oct 2015
Product Stability Testing Program - Designing and Sustaining New and Existing Programs
Oct 2015
Air Medical Transport Conference (AMTC)
Oct 2015
Computer System Validation - Reduce Costs and Avoid 483
Oct 2015
COPD
Oct 2015
Medical Device Export Approvals and Certificates in compliance with FDA regulations
Oct 2015
A look at 510(k) changes
Oct 2015
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
Oct 2015
Combination Products: FDA`s Final Rule for GMP Requirements and Introduction and Expectations for `Combo` Products
Oct 2015
Health Care in the Middle East Summit
Oct 2015
Humanitarian Congress Berlin
Oct 2015
GMP Validation Workshop | Learn to create your own workshop and private sessions
Oct 2015
Computer System Validation - Reduce Costs and Avoid 483
Oct 2015
Software Risk Analysis Tools for Medical Devices and Risk Mitigation
Oct 2015
Big Data in Clinical Development
Oct 2015
Personalized Medicine and Its Impact in the Clinic
Oct 2015
Risk Management in Clinical Trials
Oct 2015
Establishing an FDA-Compliant UDI System
Oct 2015
Human Factors and Design Controls for Medical Devices and Combination Products
Oct 2015
Orphan Medicinal Product Designation in the EU
Sep 2015
Risk-based Supplier Management System: ImpactImpact on Regulatory and Operational Goals for Medical Device Manufacturers
Sep 2015
ABHI Regulatory Conference
Sep 2015
Product Risk Management - ISO 14971:2007
Sep 2015
Compliance Software Solutions for Medical Devices
Sep 2015
Marketing Products without Getting Hammered by FDA
Sep 2015
How to Prepare for an FDA Meeting: Making the Most of Pre-IND/IDE, pre-NDA and Other Critical Meetings
Sep 2015
Conducting Effective Quality Audits: Beyond Audit Checklists
Sep 2015
Cleaning Validations Using Extraction Techniques
Sep 2015
Budgeting for Clinical Trials: Understanding Costs of a Study and Which Costs Sponsors are Responsible to Cover
Sep 2015
The Role of FDA in Health Care Software Regulations and Development
Sep 2015
Annual Open Innovation for the Life Science Sector
Sep 2015
World Congress and Expo on Medical Devices
Sep 2015
Creating Design History Files (DHF), the Device Master Records (DMR) and the Device History Records (DHR), Utilizing the Principles of Lean Documents and Lean Configuration
Sep 2015
The New Medical Device Regulation Information Day
Sep 2015
Designing Medical Devices for Long Life at Lower Costs
Sep 2015
Medical Device Regulation in Asia/Pacific Markets
Sep 2015
Marketing Products without Getting Hammered by FDA
Sep 2015
FDA 510(k) Requirements, Submission, and Clearance: Best Practices
Sep 2015
Application of Lean Six Sigma Methodology for Regulated Industries
Sep 2015
Auditing QC and Contract Laboratories for GMP Compliance
Sep 2015
Medical Grade Polymers
Sep 2015
Conformance of Design History Files for Mature Medical Devices
Sep 2015
The FDA’s DHF, DMR and DHR Design Dossier for Documentation
Sep 2015
FDA`s enforcement of 21 CFR part 11 compliance
Sep 2015
Basic Requirements for Developing IQ and OQ Protocols
Sep 2015
China Xiamen International Health Industry Expo
Sep 2015
Computer System Validation - Reduce Costs and Avoid 483s: 2-day In-person Seminar
Sep 2015
Understanding the Implications of FDA 483s and Actions to Avoid Further Regulatory Actions
Sep 2015
Smart Healthcare Technology Summit
Sep 2015
Mobile in Clinical Trials
Sep 2015
Cancer Diagnosis & Therapy Congress
Sep 2015
MEDevice San Diego Conference and Technology Showcase
Sep 2015
CAPA Investigations - Tools for a Compliant and Effective Investigation Process
Sep 2015
Annual Market and Patient Access in Latin America
Aug 2015
International High Technology of XXI Innovations on SCO Space
Aug 2015
Getting to Know FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies
Aug 2015
Global Forum on Research and Innovation for Health
Aug 2015
Meeting Annual U.S. FDA cGMP Training Requirements
Aug 2015
Key Considerations in Verification & Validation of Medical Devices
Aug 2015
Advanced Sales & Marketing in Health China
Aug 2015
Promotion of Biomedical Products: Regulatory Considerations
Aug 2015
Medical Device Reporting (MDR)
Aug 2015
Introduction to Medical Combination Products
Aug 2015
International Conference and Expo on Audiology and Hearing Devices
Aug 2015
PREPARING FOR IMMINENT FEDERAL HIPAA AUDITS (LEVEL:ADVANCE)
Aug 2015
Preparing for Imminent Federal Hipaa Audits (level:intermediate)
Aug 2015
Medical Device Registration & Listing, and Inspection Follow-up Activities
Aug 2015
The Statistics of: Design Verification, Process Validation, and Statistical Process Control
Aug 2015
Supplier Quality Agreements - Essential for Suppliers of Many Outsourced Processes
Aug 2015
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs
Aug 2015
How To Conduct Medical Device Risk Analysis Effectively (level: Advance)
Aug 2015
Pharmaceutical Congress Asia (PharmaCon)
Aug 2015
Failure Mode and Effects Analysis for Design Improvement and Design Control
Aug 2015
Understanding the Mobile Medical Applications Guidance
Aug 2015
How to Survive an FDA Inspection
Aug 2015
European Filing and Registration Procedures
Jul 2015
Risk Reduction against Regulatory Enforcement by the Investment Advisory Community Panel
Jul 2015
Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
Jul 2015
Research Instruments and Equipment Expo & Conference
Jul 2015
FDA Inspection and Medical Device Design Control
Jul 2015
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions
Jul 2015
How to get a CLIA Waiver for your Medical Device
Jul 2015
Applied Statistics for QA, QC, Manufacturing, and Design Control at SFO
Jul 2015
Applied Statistics for Scientists and Engineers at Boston
Jul 2015
Market Access and Commercial Strategy for Healthcare Industry
Jul 2015
Asian IVD Congress & Exhibition Indonesia
Jul 2015
Additive Manufacturing
Jul 2015
Cyber Security for Healthcare Summit
Jul 2015
Additive Manufacturing for Medicine and Dentistry
Jul 2015
DIA-TOPRA Workshop on Adaptive Pathways
Jun 2015
Medical Device Summit West
Jun 2015
The Secrets of Successful Medical Development Process
Jun 2015
South East Asia Regulatory Compliance for Life Science Products, Live Webinar
Jun 2015
Failure Mode & Effects Analysis for Design Improvement & Control for Medical Devices, Live Webinar
Jun 2015
Designing Medical Device Alarms to Mitigate New FDA Concerns
Jun 2015
A CAPA Primer - Elements of a CAPA Program
Jun 2015
How to Develop PAT Approach-Regulatory Compliance
Jun 2015
Connected Health Devices
Jun 2015
International Product Registration: What documents are required?
Jun 2015
U.S. FDA`s New Strategic Priorities 2014 - 1018 ()
Jun 2015
Clinical Trial Guidelines & the New Clinical Trial Regulation
Jun 2015
Effective Complaint Handling, Medical Device Reporting and Recalls - Avoiding Costly Errors:
Jun 2015
Point-of-Care Diagnostics Conference
Jun 2015
Learning from Recent FDA Warning Letters Related to Part 11 and Computer Validation
Jun 2015
Patient Centric Clinical Trials Europe
Jun 2015
Conducting Observational Studies in US, Canada and Europe
Jun 2015
Quality by Design: Establishing a Systematic Approach to Pharmaceutical Development
Jun 2015
How to Most Effectively Prepare for and Manage FDA Inspection: Best Practices
Jun 2015
Life Sciences Trainers and Educators Network Annual Conference (LTEN)
Jun 2015
ReaTech Italia
May 2015
Wearables Europe
May 2015
Establish and Maintain an Effective Supplier Qualification Program
May 2015
The FDA Inspection: Preparation, Management, and Follow-Up
May 2015
Developing and Using the Product Risk Management File/Report
May 2015
How to Conduct Medical Device Risk Analysis Effectively
May 2015
Crash Course in EU Medical Device Law for Pharma Professionals
May 2015
An Introduction to Medical Device Software: Regulations & Requirements
May 2015
CAPA, Failure Investigation and Root Cause Analysis - FDA Expectations
May 2015
Practical Application of HIPAA Risk Analysis
May 2015
Managing FDA After a Bad Inspection
May 2015
Design History File (DHF), Device Master Record (DMR) and DHR Utilizing the Principles of Lean Documents and Lean Configuration
May 2015
The A to Z`s of Writing and Enforcing Effective SOPs (Standard Operating Procedures)
May 2015
Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR
May 2015
Part 2 - Quality Management System effectiveness: ICH Q10 principles, impact of failure on COGS, principles of QRM, what you can impact in reactive versus proactive
May 2015
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements
May 2015
Complaint Handling in Compliance with FDA and ISO Regulations
May 2015
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions
May 2015
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU
May 2015
MEDTEC France
May 2015
FDA Guidance on RUO (Research Use Only)/IUO (Investigational Use Only) Products
May 2015
FDA Inspections: Before, During and After
May 2015
What Device Firms Should Know about Design Control for an Adequate Implementation
May 2015
Cosmetex
May 2015
International Conference on Significant Advances in Biomedical Engineering
Apr 2015
MDRs - Bureaucracy or Benefit
Apr 2015
ICH Q10 - Reading the Crystal Ball How will the Pharmaceutical Quality System impact the cGMPs
Apr 2015
DesignMED Europe
Apr 2015
HIPAA Audit Program Update
Apr 2015
Case Studies from the Heart of Manhattan
Apr 2015
Personalized Medicine World Conference UK (PMWC)
Apr 2015
Change Control - Key to Successful cGMP Compliance
Apr 2015
UDI Implementation
Apr 2015
South East Asia Regulatory Compliance for Life Science Products - Hong Kong, Taiwan, Thailand, Singapore, Malaysia and Vietnam
Apr 2015
Electronic Records and Signatures - 21 CFR Part 11: Basic Concepts
Apr 2015
Writing and Implementing Statistical Analysis Plans (SAPs) - Domestic and International Guidance under ICH E9
Apr 2015
Quality System Regulations for Devicemakers: A Regulatory Approach
Apr 2015
Medical Packaging Validation Strategies, Planning for Success
Apr 2015
cGMPs in the Quality Control Laboratory
Apr 2015
The Need and Role of Standard Operating Procedures in the Pharmaceutical and Medical Device Industries
Apr 2015
Combination Drug/Device Products CGMPs - Final Rule
Apr 2015
The Values and Benefits of Medical Device Reporting Compliance
Apr 2015
Innovations in Valve and Structural Heart Disease
Apr 2015
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Apr 2015
How to Achieve 510(k) Application Success for Device Software: Avoid Pitfalls that Could Delay Your Market Entry
Mar 2015
Health Canada’s Enforcement of the Regulatory Requirements for the Manufacture, Advertising and Sale of Pharmaceuticals, Medical Devices and Natural Health Products
Mar 2015
HIPAA and BYOD - Portable Devices and Enforcement
Mar 2015
ICNBS Egypt
Mar 2015
Product Standards, Menthol and FDA`s Deeming Regulation
Mar 2015
Knowledge Management (KM) Dublin
Mar 2015
New Part 11 Guidance for Clinical Trials: What This Means for You
Mar 2015
Designing Effective and Efficient Extractables or Leachables Studies for Biologics
Mar 2015
Biological Facility Design for Compliance
Mar 2015
Biomedical Software Regulation
Mar 2015
Medical Device Product Development Process
Mar 2015
annual Government Programs Summit
Mar 2015
Avoid Warning Letters in View of the U.S. FDA`s Stated Goal
Mar 2015
Pre-Filled Syringes
Mar 2015
Effective Complaint Handling, Medical Device Reporting and Recalls
Mar 2015
Missing Data in Clinical Trials
Mar 2015
Forecasting and Optimization of the Clinical Supply Chain Summit
Mar 2015
Lean, Six Sigma, Kaizen and QbD Life Science Summit
Mar 2015
Applied Statistics for Scientists and Engineers
Mar 2015
Regulatory Compliance for Dietary Supplements in the US, EU and Canada
Mar 2015
Newest Developments in Medical Diagnostics & Therapy for All Health Professionals
Mar 2015
Better Alternatives to Sampling Plans
Mar 2015
LAA Asia Pacific
Mar 2015
Marketing Products Without Getting Hammered by FDA
Mar 2015
Institutional Review Boards (IRBs): The Changing Landscape and the Effect on the Conduct of Clinical Research
Mar 2015
MEDTEC UK
Mar 2015
How to Avoid an FDA Warning Letter with a Strong CAPA Program
Mar 2015
Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Pharmaceutical Water Systems
Mar 2015
Complaint Handling and Management: From Receipt to Trending
Feb 2015
Coupon & Co-Pay Strategy, Tracking, and Compliance
Feb 2015
Regulatory Filing Strategies Summit
Feb 2015
The International Partnering of the Israeli BioMedTech Industry Life Sciences Israel
Feb 2015
Medical Device & Diagnostic Sales Training - Conference
Feb 2015
Medical Device & Diagnostic Clinical Education Conference
Feb 2015
Annual Medical Device Hospital Procurement & Payer Forum
Feb 2015
Engineering Expo
Feb 2015
Effective and Efficient Internal and Supplier Quality System Auditing for Medical Devices
Feb 2015
The 6 Most Common Problems in FDA Software Validation and Verification
Feb 2015
FDA Quality System Management for Medical Devices
Feb 2015
Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials
Feb 2015
Health Technology Management Seminar
Feb 2015
Clinical Trial Liability Lawsuits
Feb 2015
Blinding of Investigational Materials
Feb 2015
The FDA Medical Device Approval Process: Preparation of 510(k)s, IDEs, PMAs
Feb 2015
The FDA 510(k) and Q-Submission: Best Practices
Feb 2015
FDA proposed changes to ISO 13485: and Medical Devices Quality Management Systems
Jan 2015
Pre-Filled Syringes
Jan 2015
Benchmark for Cleaning Validation
Jan 2015
EU Clinical Trial Regulation: New Requirements
Jan 2015
U.S. FDA`s Strategic Priorities - and Beyond
Jan 2015
QUANTITATIVE EVALUATION AND MANAGEMENT of Cross Contamination Risks in Multi-Product Facilities
Jan 2015
Medifest South Africa
Dec 2014
Device Corrections and Removals
Dec 2014
Hands-On Peripheral Venous & Arterial Imaging, Including Vascular Access
Dec 2014
Developing an Efficient Relationship with FDA
Dec 2014
Hands-On Carotid & Vertebral Duplex Imaging
Dec 2014
Disposables for Biomanufacturing Asia
Dec 2014
Wireless Medical Devices Conference
Dec 2014
Managing Product Recalls in Accordance with Part 806
Dec 2014
In Vitro Diagnostic Directive (IVDD)
Nov 2014
Clinical Project Management
Nov 2014
Clinical Research Training for Junior CRAs
Nov 2014
Special Considerations during Medical Device Design: Dos and Don`ts
Nov 2014
BIT`s Annual International Conference of Medichem (ICM)
Nov 2014
ISO 13485 for Medical Devices
Nov 2014
International Congress on Medicinal Science and Technology (ICMST)
Nov 2014
LifeScience Alley Conference & Expo
Nov 2014
Health IT & Investment Congress and Exhibition
Nov 2014
Medical Asia
Nov 2014
Clinical Trial Inspections: Preparing for a Good Outcome
Nov 2014
ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements
Oct 2014
How to Develop an Effective Compliance Program
Oct 2014
Labelling Compliance and UDI Implementation for Medical Devices and IVDs
Oct 2014
Points of Consideration during Medical Device Design and Development - Dos and Donts
Oct 2014
Quality System Regulations for Drugs, Devices, and Tablets and How to generate your DMF
Oct 2014
Legacy System Replacement in an FDA-Regulated Environment
Oct 2014
Regulatory Affairs in Emerigng Markets
Oct 2014
Global eSubmissions
Oct 2014
International Conference on Medical Information Technology and Biomedical Engineering (MITBE)
Oct 2014
International Forum Complex support of laboratories (LAB CompLEX)
Oct 2014
Anticipation and Expectations of a Medical OEM Design Control Audit
Oct 2014
Innovations in Medicine Conference
Oct 2014
Risk Management in Clinical Research
Oct 2014
Legal Basics for Clinical Study Contracts
Oct 2014
Outsourcing in Clinical Trials New England
Oct 2014
Texting and E-mail with Patients — Communicating Within the HIPAA Rules
Oct 2014
The Pregnancy Summit
Oct 2014
CIO Life Sciences Summit
Oct 2014
Implementing the Best Practices for FDA Inspection Preparation and Management
Oct 2014
Validate Your Own Excel Spreadsheet Application - Workshop
Oct 2014
Clinical Research for Clinical Trial Assistants
Oct 2014
CUKUROVA MEDICINE
Sep 2014
Effective Complaint Handling, Medical Device Reporting and Recalls and Avoiding Costly Errors
Sep 2014
General Introduction to Clinical Research
Sep 2014
Effective Complaint Handling, Medical Device Reporting and Recalls and Avoiding Costly Errors
Sep 2014
Pharma Anti-Counterfeiting & Serialization
Sep 2014
Point of Care Diagnostics
Sep 2014
Polymers in Drug Delivery Devices
Sep 2014
Polymers in Drug Delivery
Sep 2014
Quality Management System for Practical Wholesalers
Sep 2014
Human Factors Engineering
Sep 2014
Indian Lab Automation (ILA)
Sep 2014
Hospital St. Petersburg
Sep 2014
Biomarker Utilisation & Commercialisation
Sep 2014
Global Clinical Trials
Sep 2014
FDA Regulations for Food, Drugs, Biologics, Cosmetics, and Medical Devices Including IVDs
Sep 2014
International Conference on Medical and Bioengineering (ICMBE)
Sep 2014
International Conference on Radiology and Imaging
Sep 2014
Current Good Manufacturing Practices (cGMP) for Medical Devices and IVDs
Sep 2014
Combined Scientific Meeting (CSM) on Imaging and Radiation in Personalised Medicine
Sep 2014
Global Medical Device Regulation: US, EU and Canada at Chicago IL
Sep 2014
FDA Recordkeeping Requirements
Aug 2014
Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration
Aug 2014
Maintaining a Validated State – PV, PM and Statistics associated with Current Regulation
Aug 2014
MEDITECH -International Health Fair
Aug 2014
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements
Aug 2014
Statistical Considerations for ICH Guidelines
Aug 2014
Annual Sustaining Effective CAPA Systems
Jul 2014
Auditing, Qualifying and Controlling, Suppliers and Contractors for Pharmaceuticals and Medical Devices (Purchasing Controls)
Jul 2014
FDA’s Part 11 – Enforcement Trends and Affordable Steps to Take Today
Jul 2014
Cleaning, Maintenance and Calibration Programs: Critical Programs but Often Overlooked
Jul 2014
Understanding and Implementing the Medical Device Directive
Jul 2014
How to Host Regulatory Audits (FDA, EU and Health Canada)
Jul 2014
HIPAA Fundraising: What You Need to Know, What You Need to Do
Jul 2014
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
Jul 2014
Conducting an Effective Quality System Management Review
Jul 2014
21 CFR Part 11 Add-On Inspections by the FDA
Jul 2014
Basic Components of Establishing Quality Agreements
Jul 2014
Analyzing Your Biggest Data - Practical Text Mining for Regulated Companies
Jul 2014
Risk Analysis: How to Do it Right under HIPAA and HITECH
Jul 2014
Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data
Jul 2014
Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions
Jul 2014
Integrating Risk Management into the CAPA System
Jul 2014
California Healthcare Transactions
Jul 2014
mHealth in the Pharmaceutical Industry
Jul 2014
Simulating Clinical Trials Using The FACTS Software Package
Jul 2014
FDA Guidance: Medical Device Recalls
Jul 2014
To file or not to file an NDA Application: When GCP Noncompliance Compromises your Pivotal Trial
Jul 2014
CardioVascular Clinical Trialists (CVCT) Asia Forum
Jul 2014
FDA Guidance Design Considerations for Pivotal Clinical Investigations for Medical Devices
Jul 2014
The 510(k): Its Purpose, Compilation, and Submission
Jul 2014
OneMedForum New York
Jun 2014
OPTIROB - International Conference on Aerospace, Robotics, Manufacturing Systems, Mechanical Engineering, Biomechanics, Neurorehabilitation, Human motricities
Jun 2014
Creating a value-added Internal Auditing system
Jun 2014
Best Practices With Submissions Under Medical Device User Fee Act (MDUFA)
Jun 2014
Annual PCT (Partnerships in Clinical Trials) MENA and Turkey
Jun 2014
Global Pharma Manufacturing Summit
Jun 2014
Medical Device Software Risk Management and Assurance Case
Jun 2014
Precision Diagnostics Summit
Jun 2014
Global Pharma Crisis Communication & Media Management Summit (GPCC)
Jun 2014
Pharmacovigilance System Master File & Inspections
Jun 2014
Medical Device and IVD Regulations in Asia Pacific
Jun 2014
Partnerships in Medical Device Trials Conference
Jun 2014
InnoMateria
May 2014
Sample Prep
May 2014
Medical Devices - European Regulatory and Market Access Trends
May 2014
BioDevice
May 2014
Preparing for FDA BIMO Inspection and Management
May 2014
MediCare
May 2014
Establishing a Medical Device Complaint Handling System integrated with a UDI System
May 2014
SuperFactorry
May 2014
FDA GMP Requirements For Medical Devices - The Quality Management System
May 2014
GCP and Quality in Clinical Trials
May 2014
Submitting FDA Electronic Regulatory Filings – Drug Establishment Registrations and Drug Listings
May 2014
Medical Device Reporting (MDR)
May 2014
M-Health World
May 2014
Successful Medical Device and IVD Post Market Surveillance and Vigilance Reporting
May 2014
Annual European Clinical Data Forum
May 2014
Testing Medical Devices for Efficiency and Efficacy
May 2014
MD and M Texas MedTech Event
May 2014
CHI`s Biologics Formulation & Delivery Summit
May 2014
Implementing a Medical Device Reporting (MDR) System Integrated with a UDI System
May 2014
FDA Warning Letter Close-Out Program
May 2014
Meet FDA Expectations for a Tougher Supplier Audit Program
May 2014
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
May 2014
REHATECH
Apr 2014
HIPAA Risk Analysis - Techniques to Find and Manage Security Risks
Apr 2014
Companion Diagnostics: From Biomarker Identification to Market Entry
Apr 2014
Adverse Event Reporting Compliance:The Key to Safe Drug Development / Subject Safety
Apr 2014
Implementing a Unique Device Identification (UDI) System - Issued on 2013
Apr 2014
Design Change Analysis – Four Considerations
Apr 2014
The U.S. FDA`s CAPA
Apr 2014
China International Medical Equipment Exhibition
Apr 2014
Device Design for Pharma Directors and Product Managers
Apr 2014
Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820
Apr 2014
Transferring Medical Device Production to a Contract Manufacturer - Decision Making Process and Procedures
Apr 2014
Clinical Evaluations & Investigations for Medical Devices
Apr 2014
Mobile & Wearable Technology: Healthcare
Apr 2014
Polymeric Materials in Medical Device
Apr 2014
MEDICAL DEVICE CLINICAL STUDIES - Understand How to Conduct Pre and Post Market Medical Device Clinical Studies
Apr 2014
Fundamentals of Clinical Outsourcing Certificate Program
Mar 2014
Aseptic Surgery Forum
Mar 2014
Mastering the HIPAA Privacy, Security, and Breach Notification Rules: Coping with Rule Changes, Managing Incidents, Preparing for Audits, and Avoiding Penalties
Mar 2014
Clinical Trial Applications in Canada, and Comparison to US and EU
Mar 2014
Pre-Filled Syringes - Advances in Manufacture - Pre-Conference Workshop
Mar 2014
OrthoTec Europe
Mar 2014
Best Practices for Implementing an Adverse Event Reporting System for Medical Devices Including IVDs
Mar 2014
Annual Pharma & Medical Device Nordic Market & Patient Access Forum
Mar 2014
Cell Culture Asia
Mar 2014
Ensuring 21 CFR 11 Compliance at Suppliers
Mar 2014
Understanding ISO 13485 vs. ISO 9001 for Successful QMS in Medical Device Industries
Mar 2014
Excellence in Diabetes
Mar 2014
Implementing Risk Management Principles and Activities within a Quality Management System
Feb 2014
Annual Medical Device Directive and the Recast
Feb 2014
Annual Temperature Maintenance of Pharmaceuticals in Distribution
Feb 2014
Regulatory Information Management
Feb 2014
Key Regulatory Documents: Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) and Design Dossier
Feb 2014
Learning from FDA Warning Letters
Feb 2014
Medical Device Changes and the 510(k)
Feb 2014
RoHS2 Compliance for Medical Devices
Feb 2014
Good Documentation Practices for Clinical Trials
Feb 2014
Annual Biomanufacturing Summit
Jan 2014
Effective Root Cause Analysis: The key to an effective corrective actions system
Jan 2014
Understanding Crucial Issues in the 510(k) Process
Jan 2014
The Sunshine Act - Are You Prepared? The Reporting Deadline is Approaching Quickly!
Jan 2014
HIPAA Enforcement and Compliance Audits: What the auditors want and how to be ready before they call
Jan 2014
Global Clinical Outsourcing Forum
Jan 2014
SETCOR International Conference of Smart Materials and Surfaces (SMS Bangkok)
Dec 2013
Wireless Connectivity in Medical Devices
Dec 2013
Sample Prep East
Dec 2013
Development of a Pre-filled Syringe System
Dec 2013
BiSpecifics: Concept to clinic
Dec 2013
Wireless Medical Devices - West
Dec 2013
European Clinical Data Management Forum
Dec 2013
Healthcare Management Asia
Dec 2013
2-day In-person Seminar: Why is FDA at my facility, and what do I do during an inspection?
Dec 2013
Conference On Instrumentations & Biotechnologies (CIB)
Nov 2013
Novel Drug Delivery System (NDDS) and Clinical Trial Management China
Nov 2013
Annual Elective Surgery Redesign Conference
Nov 2013
Annual Partnerships in Clinical Trials Congress (PCT)
Nov 2013
Clinical Trial Design for Personalised Medicine Webinar
Nov 2013
Clinical Outsourcing for Medical Devices
Nov 2013
Medical Device Agreements: M&A, Licensing, Co-Development, and Collaborations
Nov 2013
Medical Device Change(s), Analysis and 510(k) Impact
Nov 2013
Bringing Compliance To Design Control For Older Products
Nov 2013
Social Media and Marketing FDA Regulated Products
Nov 2013
The Sunshine Act - Have you seen the light?
Nov 2013
Validations and Resolving Problems Related to Them
Nov 2013
FDA vs. EU Inspections - How to Prepare and What are the Differences
Nov 2013
Robust Corrective And Preventive Action (CAPA)
Nov 2013
Changes to the 510(k) System - Impact on Innovation, Investment, and Business Development: One and a half day In-person Seminar
Nov 2013
Medic East Africa
Nov 2013
Supplier Quality Agreements for Medical Devices
Nov 2013
Clinical Trial Supply (CTS)
Nov 2013
510(k) for IVDs
Nov 2013
Corrective and Preventive Actions(CAPA) - 8 Steps to Achieve Compliance
Nov 2013
Unique Device Identification (UDI) Final Rules Overview
Nov 2013
Annual FDA Boot Camp Devices Edition
Nov 2013
Thorough and Complete Investigations and Follow-up - A Current Regulatory Expectation
Oct 2013
MD&M Minneapolis Expo & Conference
Oct 2013
Process Capability Indices in Medical Device Manufacturing
Oct 2013
IEEE International Conference on Imaging Systems and Techniques (IST)
Oct 2013
Creating a Good Design History File (DHF) for Audit Success
Oct 2013
Naidex South
Oct 2013
Saint-Petersburg International Health Forum
Oct 2013
Charging for Investigational Drugs: Current Application of 21 CFR Part 312 and the Expanded Access Rules
Oct 2013
National Pathology Forum
Oct 2013
Falsifying Data in clinical trials. What to report?
Oct 2013
Annual Forum on Sunshine Act Compliance & Aggregate Spend Reporting
Oct 2013
Post Approval Studies
Oct 2013
Disposable Solutions for Biomanufacturing Summit USA
Oct 2013
Risk Management for Medical Devices: ISO 14971:2007
Oct 2013
MEDTEC India
Oct 2013
WIHE Hospital - Warsaw International Healthcare Exhibition
Oct 2013
MDiT Forum and Regulation Summit
Sep 2013
Design of Implantable Devices Conference
Sep 2013
OrthoTec China
Sep 2013
European AAATE Conference - Association for the Advancement of Assistive Technology in Europe
Sep 2013
Software Validation for the New FDA Inspections
Sep 2013
Naidex Scotland
Sep 2013
Global Anti-Corruption and Corporate Compliance for Pharma
Sep 2013
Inhalation Drug Delivery
Sep 2013
Clinical Trial Supply USA
Sep 2013
International Conference on Instrumentation, Control and Automation
Aug 2013
Asia Global Fair
Aug 2013
China International In Vitro Diagnostics Technology and Industry Development Summit (IVDS)
Aug 2013
FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes
Aug 2013
Singapore International Healthcare Expo
Aug 2013
Singapore International Healthcare Week
Aug 2013
Coping with a Difficult Compliance Officer when Responding to a 483, Warning Letter, Import Alert or Recall
Aug 2013
Regulatory Differences Between Biopharmaceutics and Medical Devices
Aug 2013
Medical Device Global Labeling Strategies Conference
Jul 2013
Annual Asian Patient Access Leaders Forum
Jul 2013
Unlocking Potential in Drug Portfolios Through Rx to OTC Switch
Jul 2013
How to Manage a Medical Device Recall Efficiently and Effectively
Jul 2013
Construct and Manage the Technical File and Design Dossier
Jul 2013
CAPA – The Heart of Your Quality System
Jul 2013
Software Validation for the New FDA Inspections
Jul 2013
Supplier Management – Do you comply with the latest FDA and ISO 13485 requirements
Jul 2013
Clinical Trial Regulatory & Guideline Requirements
Jul 2013
Medical Device Manufacturing and R&D Summit
Jun 2013
Optimal capacity planning and resource allocation for a portfolio of clinical trials
Jun 2013
Good Manufacturing Practice (GMP) Annual Training
Jun 2013
The Future of Off-Label Marketing After the Caronia Decision
Jun 2013
MedTech Innovate Seminars
Jun 2013
Translational Medicine Business Summit
Jun 2013
FDA and Social Media - How to Promote your Products Using Web 2.0 in Compliance with FDA and FTC Laws and Regulations
Jun 2013
Introduction to Bioequivalence and Therapeutic Equivalence
Jun 2013
Shared facilities and the move to science based risk assessments
Jun 2013
Clinical trial regulations, GCP compliance and FDA inspections
Jun 2013
Serious Product Quality Problems – Dealing with the Press and the Public
Jun 2013
Ethio Health Exhibition & Congress
Jun 2013
FDA Warning Letter Closeout Program
May 2013
DoD/VA Healthcare
May 2013
Complaint Systems – The Essential Requirements
May 2013
Pharmaceutical and Medical Packaging
May 2013
International Congress On Ultrasonics (ICU)
May 2013
Midlands Design & Manufacturing
May 2013
CIMEX - Congo International Medical Expo
Apr 2013
Conducting Successful FDA Meetings to Negotiate Product Development and Approval: 2-day In-person Seminar
Apr 2013
Regulatory Information Management
Apr 2013
Software Verification and Validation Planning to Meet FDA Requirements
Apr 2013
Overview of Combination Product Development for Pulmonary Drug Delivery
Apr 2013
Interactive Response Technologies for Clinical Trials
Apr 2013
Best Practices for Preparation for, Behavior during, and Response to an FDA Inspection
Apr 2013
Medical Device Labeling (In-Vitro Lab “Home Brew” off - Label Guidance & Enforcement): 2-day In-person Seminar
Apr 2013
Medical Devices: Designing and Implementing a Reimbursement Strategy Geared Toward CMS Reimbursement Approval
Apr 2013
Design of Medical Devices Conference
Apr 2013
DHF, DMR, DHR and TF - Regulatory Documents Explained
Apr 2013
Best Practices for Conducting OOS Investigations (in Pharmaceutical Laboratories)
Apr 2013
The World Congress Annual Leadership Summit On Mergers & Acquisitions (M&A)
Apr 2013
Auditing the QC Microbiology Laboratory for FDA Compliance
Apr 2013
Key Factors to develop an effective CAPA system
Apr 2013
MedExpo Saudi Arabia
Apr 2013
When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation
Apr 2013
3-hr Virtual Seminar: Annual ICH GCP Refresher Course
Apr 2013
FDA Inspections - How Investigators Typically Process the Results
Apr 2013
Defining And Managing User Requirements For Computer System Validation
Mar 2013
Life Sciences Market Research
Mar 2013
Raw Materials Risk Management in GMP Facilities: Avoiding GMP non-Compliance Due to Raw Material Issues
Mar 2013
Global Medical Device Reporting - A Comparison of Worldwide Regulations
Mar 2013
Forecasting Clinical Study Enrollment and its Budget Considerations
Mar 2013
FDA`s Import Requirements and Managing the Import of FDA Regulated Products: 2-day In-person Seminar
Mar 2013
21 CFR Part 11 Electronic Records: Electronic Signatures
Mar 2013
Best Practices in Document Approval, Control, and Distribution
Mar 2013
Obtaining Faster FDA 510(k) Approvals - The 510(k) as an Advocacy Document: One and a Half-day In-person Seminar
Mar 2013
Transferring a Medical OEM Molding and Assembly Operation to a Manufacturer With Validated Systems and Processes
Mar 2013
Seeking Evidence in Clinical Trials in Hemoglobinopathy
Mar 2013
Electronic Records & Electronic Signatures; 21 CFR Part 11
Mar 2013
FDA Medical Device Approval Process (510(k), IDE, PMA)
Mar 2013
Design Controls - Requirements for Medical Device Developers
Mar 2013
Annual Pharmaceutical & Medical Device Pricing & Reimbursement in Turkey
Mar 2013
The 510(k) Submission: Requirements, Contents, and Options
Mar 2013
Curtailing Microbial Excursions and Investigations in Pharmaceutical Water Systems
Mar 2013
Risk Assessment - Compliance Using Easy To Fill Out Documentation
Mar 2013
Cost reductions through single use systems
Mar 2013
Dubai Anaesthesia Conference & Exhibition
Mar 2013
FDA Warning Letters - Stop Fumbling your Response and Effectively Demonstrate Compliance
Mar 2013
You have a Sterility Failure or Bioburden Excursion - Now What?
Mar 2013
Implementation and Utilization of Standard Operating Procedures (SOPs) at the Clinical Research Site
Mar 2013
Why are we seeing more Independent Data Safety Monitoring (DMC) use in Clinical Research
Mar 2013
Medical Device Summit
Mar 2013
American Healthcare and Natural Products Expo
Mar 2013
FDA`s 21 CFR 11 Add-On Inspections - Recent Updates
Feb 2013
Maximizing the Performance & ROI in Clinical trials: A Personalized Approach
Feb 2013
Ensure Compliance to FDA`s Design Control Requirements by using Requirements Management Techniques
Feb 2013
Risk-based Software Validation for Quality System software and Medical Device Data Systems (MDDS)
Feb 2013
Medicaid Drug Rebate Program (MDRP): A Primer
Feb 2013
Clinical Study Enrollment Metrics and Their Financial Impacts
Feb 2013
Outsourcing Management - Effective Contract Manufacturers, Supplier Evaluation, Approval and Monitoring
Feb 2013
Purchasing and Supplier Controls in the Medical Device Industry
Feb 2013
ISO 13485 - Medical Devices: Quality Management Systems
Feb 2013
Improve Supplier Quality (for Clinical Trial Projects) - Learn How to Implement a Robust Request for Proposal Process
Feb 2013
The Caronia Court Decision and Off-Label Promotion
Feb 2013
Medical Device Quality Management Systems
Feb 2013
Statistics for Quality Control and Process Validation: How Many Replicates
Feb 2013
Statistics for Quality Control and Process Validation: Linear Regression and Standard Curves
Feb 2013
Using Statistics to Determine Sample Size
Feb 2013
Root Cause Analysis
Feb 2013
GMP Compliance Chapter - Change Control, Out-of Specification Investigations and CAPA
Feb 2013
Adaptive Clinical Trials - Clinical Trials Version 2.0
Feb 2013
How to Achieve CMDCAS Certification (For Medical Device Companies That Want to Sell in Canada)
Feb 2013
Effectiveness Measures in CAPA and Risk Management Plans: Applying LSS for Quality Metrics
Feb 2013
Best Practices in Responding to Form 483s
Feb 2013
Effective CAPA related to Managing Human Error
Feb 2013
Conformance of Design History Files for Mature Medical Products
Feb 2013
(Medical Claim) Modifiers: Complying with Payer Variations
Feb 2013
Social Media: Using The Legal Guideposts to Create Social Media Success (for Healthcare/Lifescience Companies)
Feb 2013
Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection?
Feb 2013
Training on Current ICH GCP Guidelines
Feb 2013
The International Conference of Personalized Medicine and Targeted Therapies in Cancer (PMTC)
Feb 2013
Assistive Technologies - (AT)
Feb 2013
Current Good Manufacturing Practice for Medical Devices Including IVDs
Jan 2013
Annual Health Outcomes and Pharmacoeconomics Research Conference
Jan 2013
Optimal Clinical Supply Planning for Global Drug Development
Jan 2013
Essentials of Sterilizing Grade Filter Validation
Jan 2013
Sampling Plans for (FDA) Quality Audits
Jan 2013
Product Complaint Investigations - The application of Lean Six Sigma methodology for U.S. FDA-Regulated Industries
Jan 2013
How to Obtain a Canadian Medical Device License
Jan 2013
Cost-Effective Computer System Validation: Step-by-Step
Dec 2012
Patient Reported Outcomes (PROs): Overview and Guidance for clinical trials and medical product labeling
Dec 2012
Responding to FDA 483`s
Dec 2012
Recalls & Vigilance - When to Report Complaints
Dec 2012
Root Cause Analysis and Documentation Requirements for CAPA
Dec 2012
Hot-Melt Extrusion for Pharmaceutical Applications
Dec 2012
Change Control - Key to Successful cGMP Compliance
Dec 2012
21 CFR Part 11: Auditing for Part 11 Compliance
Dec 2012
Pan Arab Psychiatric Conference (PAPC)
Dec 2012
Managing Your Medical Device Reporting (MDR)Program for Compliance Success
Nov 2012
Product Hazard Analysis and Risk Management Under ISO 14971 and FDA, ICH Q9
Nov 2012
Hospital Efficiency Asia
Nov 2012
Process Validation for Medical Devices
Nov 2012
Medical Device Usability and IEC 62366
Nov 2012
Medical Device Summit Europe
Nov 2012
Design Control for Medical Devices
Nov 2012
Contamination-Control and Cleaning and Disinfection
Nov 2012
Aspects to Consider for Clean Room Qualification and Operation
Nov 2012
Medical Devices Conference: Tools, Technologies, and Strategies to Accelerate Your Time to Market
Nov 2012
An Interactive Workshop on Premarket [510(k)] Notification Submissions
Nov 2012
Bullet-Proof CAPA - Webinar By GlobalCompliancePanel
Oct 2012
Artwork Origination for Pharmaceutical Packaging
Oct 2012
Health Fair Berlin Brandenburg
Oct 2012
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
Oct 2012
Computer Systems Used in Clinical Trials
Oct 2012
Process Validation for Pharmaceuticals & Medical Devices in The EU & USA - Including Practical Workshop Exercises
Oct 2012
Ciamed
Oct 2012
Reprocessing REUSABLE Medical Devices - Cleaning & Labeling Requirements
Oct 2012
Biologic Manufacturing China
Oct 2012
Avoiding 483 Observations and Warning Letters
Oct 2012
Quality Oversight Of Clinical Vendors
Oct 2012
Medifest India
Oct 2012
Pragodent
Oct 2012
Mobile Medical Applications for Devices: Trends, Bills and Guidance
Oct 2012
Risk Management: ISO14971, IEC62304 and IEC60601-1: 2005 Compliance
Oct 2012
2-day In-person Seminar: CAPA Systems for Medical Device Manufacturers
Oct 2012
Clinical Trials Drug Supply: Imports and Release Procedures for Shipping to Trial Sites
Oct 2012
Annual Meeting of the German Society of Medical Physics (DGMP) e.V.
Sep 2012
2-day In-person Seminar on Statistics for Quality Control and Assurance at New Jersy
Sep 2012
CDISC – Insight, Impact and Implementation
Sep 2012
Understanding the Decentralised and Mutual Recognition Procedures
Sep 2012
Optimising EU Reimbursement For Medical Devices - How to Build Value and Drive Reimbursement In The UK, Germany and France
Sep 2012
MEDTEC Italy
Sep 2012
IRAQ HEALTH EXHIBITION
Sep 2012
Clinical Trial Billing - Building a Compliant Process that Works!
Sep 2012
Medical Device Regulations in Europe
Sep 2012
Post Market Surveillance for Medical Devices
Sep 2012
Medipharm Tanznania
Sep 2012
MEDYCYNA XXI
Sep 2012
21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection
Sep 2012
Risk Assessment-Compliance Using Easy To Fill Out Documentation
Sep 2012
Hazard Analysis – A practical guide
Sep 2012
Clinical Trials in Asia (CTA)
Sep 2012
Global Medical Device Regulations - US, EU, Canada, Argentina, Australia, Brazil, India, Japan, Mexico, Russia, South Korea, Taiwan
Sep 2012
SPIE Nanosystems in Engineering and Medicine
Sep 2012
China International Healthcare Exposition
Sep 2012
Prepare and Submit 510(k) Premarket Notification Submissions for Success
Sep 2012
Medical Device Adverse Event Reporting Systems in EU, Canada and US - Webinar By GlobalCompliancePanel
Aug 2012
Project Management for Computer Systems Validation - Webinar By GlobalCompliancePanel
Aug 2012
Key Concepts in Successful Water System Sanitization - Webinar By GlobalCompliancePanel
Aug 2012
Validation and Use of Excel Spreadsheets in Regulated Environments - Webinar By GlobalCompliancePanel
Aug 2012
Site Challenges in Conducting Investigational Device Trials
Aug 2012
Annual Pharmaceutical Regulatory Affairs Asia
Aug 2012
Management Controls Under QSR and ISO 13485 - Webinar By GlobalCompliancePanel
Aug 2012
FDA Guidelines on in Class in Man Compounds Targeting Tumor Bioenergetics from Lab Bench to Clinical Trials - Webinar By GlobalCompliancePanel
Aug 2012
Navigating the 510(k), IDE and PMA Submission and Approval Process - Webinar By GlobalCompliancePanel
Aug 2012
Human Behavior in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel
Aug 2012
Design Controls For FDA regulated industry
Aug 2012
Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel
Aug 2012
Annual Clinical Research in Emerging Countries
Aug 2012
Hazard Analysis vs. FMECA – Differences and Commonalities - Webinar By GlobalCompliancePanel
Aug 2012
CE Marking for Medical Devices Including In Vitro Diagnostic Devices - Webinar By GlobalCompliancePanel
Aug 2012
Common Problems with Software Validation Processes - Webinar By GlobalCompliancePanel
Aug 2012
RAPS Approved Seminar on Risk Management in Medical Devices Industry at Mumbai
Aug 2012
Validating Excel and Word - Webinar By GlobalCompliancePanel
Aug 2012
Avoiding 483 Warning Letters & Remediation if you get one - Webinar By GlobalCompliancePanel
Aug 2012
GMP for Phase 1 Products - Webinar By GlobalCompliancePanel
Aug 2012
Implementing a Quality Systems-Based Approach to GCP Compliance - Webinar By GlobalCompliancePanel
Aug 2012
Sterilization as a Benchmark for Cleaning Validation and Control - Webinar By GlobalCompliancePanel
Aug 2012
FDA Guidance Regarding Software Validation for Clinical Trial Management Systems - Webinar By GlobalCompliancePanel
Aug 2012
Regulatory Complaint Handling, MDR`s & Recalls - Webinar By GlobalCompliancePanel
Aug 2012
Common Sense Water System Validation - Webinar By GlobalCompliancePanel
Aug 2012
The Use and Mis-use of FMEA in Medical Device Risk Management
Jul 2012
One and a Half-day In-person Seminar: FDA Compliant GLP for Nonclinical Studies - For Pharmaceutical and Medical Device Industries
Jul 2012
Ethics and Scientific Misconduct in Regulated Studies
Jul 2012
Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies
Jul 2012
Software V&V Protocols and Documentation - Webinar By GlobalCompliancePanel
Jul 2012
Avoiding Statistical Pitfalls during Method Validation - Webinar By GlobalCompliancePanel
Jul 2012
Auditing an Active Pharmaceutical Ingredient (API) Contract Manufacturing Organization (CMO) - Webinar By GlobalCompliancePanel
Jul 2012
How to Prepare for a Tag Along Audit of CFR 21 Part 11 - Webinar By GlobalCompliancePanel
Jul 2012
Business Development Strategies For Clinical Trials Service Providers
Jul 2012
IEC 62304 for Medical Device Software Development: Steps to Compliance - Webinar By GlobalCompliancePanel
Jul 2012
The U.S. FDA`s Tougher Supplier Controls - Webinar By GlobalCompliancePanel
Jul 2012
The Drug Development Process - From R&D to Commercialization - Webinar By GlobalCompliancePanel
Jul 2012
Update On and Look Ahead At FDA’s Changes to the 510(k) Process
Jul 2012
Risk Management for Medical Devices - Webinar By GlobalCompliancePanel
Jul 2012
Good Pharmacovigilance Practice - Inspection and Audits - Webinar By GlobalCompliancePanel
Jul 2012
How to Bullet Proof your Documents from Most Commonly Cited GDP Violations - Webinar By GlobalCompliancePanel
Jul 2012
Best Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals
Jul 2012
CSI - Catheter Interventions in Congenital & Structural Heart Disease
Jun 2012
Obtaining and Marketing Your 510(k) with Today`s FDA, a 510(k) Workshop
Jun 2012
Clinical Trials Supply & Logistics Summit
Jun 2012
Medical Design & Manufacturing - MD&M Brazil
Jun 2012
cGMPs for Medical Devices, Including In Vitro Diagnostic Devices
Jun 2012
Best Practices in Telehealth and Healthcare Technologies
Jun 2012
Annual Life Sciences Market Research Conference
Jun 2012
Money in medicine
Jun 2012
RAPS Approved Seminar on Complying with GMP and cGMP Requirements: Streamlining Quality Assurance and FDA Compliance
Jun 2012
Medical Device Supplier Quality Agreements - Webinar By GlobalCompliancePanel
Jun 2012
RAPS Approved Seminar on GMP and Regulatory Expectations for Early IND Products
Jun 2012
Prepare for Tougher cGMP Compliance Audits - Webinar By GlobalCompliancePanel
Jun 2012
The U.S. FDA`s New Global Engagement Initiative - Webinar By ComplianceOnline
Jun 2012
Medical Device: Risk Assessment and Mitigation through FMEA - Webinar By ComplianceOnline
Jun 2012
Understanding Costs of a Study for Clinical Trials - Webinar By ComplianceOnline
Jun 2012
2-day In-person Seminar: Medical Device Sterilization: Corrective & Preventive Action
Jun 2012
Medical Device Postmarketing Vigilance Reporting: Update and Expectations for Manufacturers - Webinar By GlobalCompliancePanel
Jun 2012
Residual Moisture Testing of Lyophilized Products - Webinar By GlobalCompliancePanel
Jun 2012
Practical Issues with Conducting Multi-National Clinical Trials for Medical Device Approval in the US
Jun 2012
MedicReS World Congress Good Medical Research
Jun 2012
National Executive Leadership Conference on Breast Centers of Excellence
Jun 2012
Effective Corrective and Preventive Actions (CAPA): 10 Steps - Webinar By GlobalCompliancePanel
Jun 2012
China Pharma Landscape and Forecasting Workshop
Jun 2012
Annual Pharmaceutical and Medical Packaging Leadership Summit
Jun 2012
Unsolicited Drug and Device Off-Label Claims Via Social Media and Risk Management
Jun 2012
Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanel
Jun 2012
Verification and Validation (V&V) of Software in the Medical Devices - Webinar By ComplianceOnline
Jun 2012
Lean-Agile Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel
Jun 2012
Leadership in Manufacturing Contamination Control - Webinar By GlobalCompliancePanel
Jun 2012
The 21 Elements of a 510(k) - Webinar By ComplianceOnline
Jun 2012
Device Corrections and Removals
Jun 2012
What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness?
May 2012
Making Sense of FDA’s (proposed) Rules for the Development and Approval of Biosimilars
May 2012
MedSib
May 2012
PRE-FILLED SYRINGES AND ADVANCED INJECTION TECHNOLOGIES
May 2012
Pharmaceutical and Medical Device Market Access in Key Asian Markets
May 2012
An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials
May 2012
Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel
May 2012
Supplier Controls to Meet Tougher U.S. FDA Requirements
May 2012
Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
May 2012
ORTHOPADIE + REHA-TECHNIK
May 2012
The iMedicine & Mobile Life Sciences World Summit
May 2012
Medical Device Complaints, MDR’s and Recalls
May 2012
FDA Concerns on Alarm Standards and Safety
May 2012
Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
May 2012
The International Exhibition on BioPharma, Biotechnology & Equipment (BIOTECH)
May 2012
Process Analytical Technology (PAT) is more than it Seems
May 2012
Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 2012
MEDITECH
May 2012
Device Changes and the 510(k) - Webinar By GlobalCompliancePanel
May 2012
The International Conference on Health Informatics (ICHI)
May 2012
Proper Documentation of Risk Management for Compliance with ISO 14971 - Webinar By GlobalCompliancePanel
May 2012
Medical Device Quality Systems, CAPA and European Medical Device regulations
May 2012
Electronics South
May 2012
Medical Device Process Validation - Statistical Aspects - Webinar By GlobalCompliancePanel
May 2012
South Korea: Navigating the Clinical Trial and Regulatory Environment - Webinar By GlobalCompliancePanel
May 2012
Applying GMP Quality Principles To Establish A Reduced Testing Program
May 2012
DHF, DMR, DHR and TF - Regulatory Documents Explained, and Best Practices for Controlling Them
Apr 2012
Physician Payment Sunshine Act and State Sunshine Law Compliance. Are you Prepared for the New Federal Requirements and Existing State Requirements?
Apr 2012
How to Format Succinct and Comprehensive 510(k)s and PMAs
Apr 2012
How to Survive FDA`s `New` Inspection and Enforcement Practices
Apr 2012
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
Basrah International Exhibition (BIE)
Apr 2012
Good Laboratory Practice (GLP) for Non-Clinical Laboratory Studies - Application and Compliance to Ensure Safety of Biologic Therapeutics and Medical Devices
Apr 2012
2-day In-person Seminar: Introduction to Design of Experiments for Process Characterization
Apr 2012
FDA Medical Device Regulation for the Beginner
Apr 2012
BioPharma LatAm Convention
Apr 2012
REHMED-PLUS
Apr 2012
Issue Detection and Escalation in Clinical Trial Settings
Apr 2012
Off Label Product Use Discussions in Social Media
Apr 2012
How to Establish A Medical Device Quality System
Apr 2012
Validation and Use of Excel Spreadsheets in Regulated Environments
Apr 2012
A Practical Guide to Implementing the Bribery Act in the Life Sciences Sector
Apr 2012
BIT’s Annual World Congress of Biosoft
Mar 2012
BioPh Japan
Mar 2012
Medical Device Risk Management Using ISO 14971
Mar 2012
Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements - Webinar By GlobalCompliancePanel
Mar 2012
India Healthcare Congress
Mar 2012
Best Practices for Maintaining an IND and IDE Application with FDA
Mar 2012
Live webinar on Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina) By Compliance2go
Mar 2012
Unmet Medical Need Forum
Mar 2012
How To Establish An Effective Good Clinical Practice in Drugs and Medical Devices
Mar 2012
Doing Business Despite Embargoes and Sanctions: OFAC Licensing
Mar 2012
Application of CAPA to the Device Sterilization Process
Mar 2012
SUDTEC
Mar 2012
Quality Expo Texas
Mar 2012
Medical Design & Manufacturing (MD&M Texas)
Mar 2012
Auditing Computer Systems for FDA and International Compliance - Webinar By GlobalCompliancePanel
Mar 2012
Changes in the EU Medical Device Directives; 2010 Modifications and the Recast of the MDD Directives - Webinar By GlobalCompliancePanel
Mar 2012
FDA`s Rules for Financial Disclosure in Clinical Trials Clarified: New Guidance, Practical Application
Mar 2012
How to Develop, Monitor and Effectively Communicate your Risk Control Strategy - Webinar By GlobalCompliancePanel
Mar 2012
USFDA & EU Essentials of Drug Safety and Pharmacovigilance
Mar 2012
IEEE Haptics Symposium (HAPTICS)
Mar 2012
Software Verification and Validation Planning and Implementation
Mar 2012
Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada
Mar 2012
Audit/Inspection Preparedness for Clinical Research/Site Coordinators
Mar 2012
IEEE EMBS Forum on Grand Challenges in Biomedical Imaging
Mar 2012
Advanced Methods of Root Causes Analysis for ISO 14971 Risk Reduction
Mar 2012
DMR & DHR - What Is Really Required
Feb 2012
International Conference on Biomedical Engineering (ICoBE)
Feb 2012
APA International Congress on Advances in Human Healthcare Systems (Healthcare India)
Feb 2012
Telehealth, telemedicine and telecare: Introductory one-day seminar
Feb 2012
KOL and Stakeholder Engagement Europe
Feb 2012
Implement a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
Feb 2012
Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers -- Differences and Similarities
Feb 2012
IASTED International Conference on Biomedical Engineering (BioMed)
Feb 2012
Telehealth
Feb 2012
Electronics West
Feb 2012
Coeur et Diabete (7e edition)
Feb 2012
Life Sciences Internal Audit Forum
Feb 2012
Medical Device Process Validation - Statistical Considerations
Feb 2012
Product Risk Management Under ISO 14971 and FDA-ICH Q9 - Webinar By GlobalCompliancePanel
Feb 2012
Live Web Seminar Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA By compliance2go
Feb 2012
Medication adherence: Understanding the problem; engineering a solution
Jan 2012
The Evolving State of U.S. Sanctions Against Iran
Jan 2012
Introduction to the Electronic Common Technical Document
Jan 2012
Preparing for FDA GCP Inspections – Essentials for Sponsor Companies
Jan 2012
MANAGEMENT DURING MEDICAL DEVICE CLINICAL STUDIES IN EUROPE
Jan 2012
ADVERSE EVENT MANAGEMENT DURING MEDICAL DEVICE CLINICAL STUDIES IN EUROPE
Jan 2012
Clear as Mud: Obtaining & Marketing your 510(K) with Today`s FDA
Jan 2012
Live Web Seminar Design Controls: What to know when it comes to FDA regulated industry? By compliance2go
Jan 2012
Validation and use of Access Databases in FDA regulated environments
Jan 2012
Application of CAPA in (Device) Sterilization – For the Non-Expert
Jan 2012
Combat Trauma Innovation
Jan 2012
Purposeful Water and Steam System Validation – Not Just A Regulatory Requirement
Jan 2012
SOPs for Clinical Trials – Regulatory Requirement and Key to Effective Management
Jan 2012
DRUG / DEVICE & DEVICE / DRUG COMBINATIONS IN THE EU
Jan 2012
Annual IEEE Topical Conference on Biomedical Wireless Technologies, Networks, and Sensing Systems (BioWireleSS)
Jan 2012
Production and QMS Software Validation - An Excel Example
Jan 2012
Introduction to FDA Good Documentation Practices
Jan 2012
How Doctors of Chiropractic can Bill Medicare For Durable Medical Equipment and Stay Legally Compliant
Jan 2012
Live Web Seminar China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations By compliance2go
Jan 2012
Medical Design & Manufacturing (MD&M Online)
Dec 2011
LIve Webinar on ISO14000: Environmental Management - Ins and Outs of Implementation and Understanding by Compliance2go
Dec 2011
Proven Root Cause Investigation Techniques for Pharmaceutical Water Systems
Dec 2011
Live webcast on HOW TO MANAGE COMPLAINT FILES by Compliance2go
Dec 2011
Healthy Lifestyle
Dec 2011
Global Clinical Budgeting and Contracting Conference
Dec 2011
GMP Annual Training
Dec 2011
FDA MEDICAL DEVICE INSPECTIONS - Are You Prepared?
Dec 2011
Preventing Device Maintenance Related Recalls
Dec 2011
Draft Guidance for Device Industry and FDA - Postmarket Surveillance
Dec 2011
Live webinar on Excel Spreadsheet Compliance with 21 CFR 11 by Compliance2go
Dec 2011
Site feasibility and study start up
Dec 2011
Biocompatibility Testing and Evaluations for Medical Devices
Dec 2011
How To Bill Medicare For Durable Medical Equipment and Stay Legally Compliant
Dec 2011
China Sourcing Fair: medical & health products Johannesburg
Dec 2011
THE NEW ISO 14155 REQUIREMENTS FOR MEDICAL DEVICE CLINICAL STUDIES
Dec 2011
Live webinar on The 510(k) Submission Process By Compliance2go
Dec 2011
Live webinar on Applying GMP Quality Principles To a Startup a Medical Products Manufacturing Facility From Scratch By Compliance2go
Nov 2011
Pharmaceutical and Medical Device Good Manufacturing Practices - Similarities and Differences - Webinar By GlobalCompliancePanel
Nov 2011
China (Suzhou) International Biotechnology Exhibition (Bio China)
Nov 2011
Laegedage (Medical Days)
Nov 2011
Navigating 510(k) and PMA Submissions and Approvals
Nov 2011
Live webinar on Management of Customer Complaints: Receipt, Investigation, and Trending By Compliance2go
Nov 2011
Live webinar on HOW TO PERFORM PROCESS VALIDATION by Compliance2go
Nov 2011
Clinical Trials for Medical Devices Conference
Nov 2011
Live webinar on New Changes to HIPAA Rules - Their expected impact and enforcement schedule By Compliance2go
Nov 2011
Lyophilization Process Development and Cycle Design
Nov 2011
Live webinar on GMP Quality Principles Embodied in the FDA`s Quality Systems Approach to the Pharmaceutical GMP`s and ICH Q 10, Pharmaceutical Quality Systems by Compliance2go
Nov 2011
Live webinar on Design Controls: What to know when it comes to FDA regulated industry by Compliance2go
Nov 2011
The China Medical Biotech Forum (CMBF2011)
Nov 2011
THE DEVELOPMENT SAFETY UPDATE REPORT (DSUR)
Nov 2011
FROM CORE SAFETY INFORMATION TO LOCAL LABELLING
Nov 2011
Heart, Vessels & Diabetes - The European Conference (2n edition)
Nov 2011
ESSENTIAL GUIDE TO PUBLICATIONS PLANNING - Two Day Course
Nov 2011
Document Approval, Control, and Distribution: How to Develop a Compliant, Cost Effective System By Compliance2go
Nov 2011
Key Aspects of the Trial Master File and How to Pass FDA Inspection - Webinar By GlobalCompliancePanel
Nov 2011
Best Practices in Complaint Management - Webinar by GlobalCompliancePanel
Nov 2011
Draft Guidance for Device Industry and FDA - Postmarket Surveillance - Webinar By GlobalCompliancePanel
Oct 2011
Pharmaceutical & Biopharmaceutical Stability
Oct 2011
Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel
Oct 2011
Does your Equipment Program Meet Current Regulatory Expectations - Webinar By GlobalCompliancePanel
Oct 2011
Equipment Validation, Tracking, Calibration, and Preventive Maintenance - Webinar By GlobalCompliancePanel
Oct 2011
Annual European Magnufaturein Strategic Summit
Oct 2011
Live webianr on Basic and Advanced Quality Tools: What every quality professional is expected to know by compliance2go
Oct 2011
Live webinar on The FDA Inspection: Preparation, Performance, and Follow-up by compliance2go
Oct 2011
SINCE
Oct 2011
REGULATORY REQUIREMENTS FOR CLINICAL TRIALS - Including an Update on the Proposed Changes to the Clinical Trial Directive Requirements
Oct 2011
FDA ADVERSE EVENT REPORTING FOR PHARMACEUTICALS
Oct 2011
FDA`s Draft Guidance on Financial Disclosure by Clinical Investigators - Webinar By GlobalCompliancePanel
Oct 2011
Introduction to Contamination Control Master Plans - Webinar by GlobalCompliancePanel
Oct 2011
Effective Internal Auditing-Making Quality Systems More Efficient for the Medical Products Industry - Webinar By GlobalCompliancePanel
Oct 2011
Plast Imagen Mexico
Oct 2011
Medevice Design Manufacturing Spain and Biomaterials Europe Conferences
Oct 2011
Risk Management during device design according to ISO14971 - Webinar By GlobalCompliancePanel
Oct 2011
Logipharma Boston
Oct 2011
Meeting Annual U.S. FDA cGMP Training Requirements - Webinar By GlobalCompliancePanel
Oct 2011
The Drug Development Path - From R&D to Commercialization - Webinar by GlobalCompliancePanel
Oct 2011
Hybrid Quality Systems For Pharmaceuticals - Combining ICH Q7A & Part 210-211 - Webinar By GlobalCompliancePanel
Sep 2011
Industry Ireland
Sep 2011
Annual Clinical Trials for Medical Devices
Sep 2011
Good Laboratory Practice Regulations: Introduction and Strategies for Implementation
Sep 2011
PLASTEC Midwest
Sep 2011
The Intl. Conference on Computer Safety, Reliability and Security - SAFECOMP
Sep 2011
Medical Device Regulations In Asia Pacific Market
Sep 2011
Service Management Expo (SME)
Sep 2011
Understanding Risk Management in Medical Devices
Sep 2011
International Siberian Conference on Control and Communications (SIBCON)
Sep 2011
FDA Validation Requirements - Webinar By ComplianceOnline
Sep 2011
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
Sep 2011
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems-By Howard T. Cooper
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems
Sep 2011
RFID in Health Care
Sep 2011
Reliability Engineering Fundamentals for Medical Devices - Webinar By ComplianceOnline
Sep 2011
How to design A CAPA System that meets Compliance Requirements
Sep 2011
DesignMed China
Sep 2011
Ensuring Integrity and Security of Laboratory Data
Sep 2011
Responding to FDA Form 483s and Warning Letters - Webinar By ComplianceOnline
Sep 2011
Common GCP Violations and Site Mistakes - How to Avoid them
Aug 2011
Master Validation Planning
Aug 2011
Effective Hazard Analysis to meet FDA and ISO13485:2003 Risk Management Requirements
Aug 2011
Design, Planning and Conducting Effective Audits
Aug 2011
Preparing for an FDA Pre-Approval Inspection - Webinar By ComplianceOnline
Aug 2011
Device Master Record & Device History Record
Aug 2011
Design History File (DHF) Device Master Record (DMR) Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained
Aug 2011
A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11, Electronic Records, Signatures
Aug 2011
Why Post-market Pharmacovigilance trials are increasingly seen : What do they tell us and why are they important
Aug 2011
How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit
Aug 2011
Understanding the Difference: HIPAA Security Compliance Assessment v. HIPAA Security Risk Analysis
Aug 2011
ISO 13485 and medical device quality systems - practical strategies for planning, implementation and beyond
Aug 2011
How to Survive a DEA Inspection Series: Only Manufacturers and Distributors
Aug 2011
How to write Standard Operating Procedures (SOPS) & Work Instructions (Wis) that Meet and Exceed Compliance Requirements
Aug 2011
Clinical Project Management - Webinar By ComplianceOnline
Aug 2011
Creation and management of a Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean Documents and Lean Configuration
Aug 2011
Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers
Aug 2011
Vendor Qualification - Designing and Implementing an Efficient and Compliant Vendor Program
Aug 2011
Trial Master File for Research Sites: Can You Pass FDA Inspection?
Aug 2011
Full day Virtual Seminar on Pharmaceutical Stability - Webinar By ComplianceOnline
Jul 2011
BIOMED
Jul 2011
Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11
Jul 2011
Vendor Qualification Auditing for FDA Computer System Compliance - Webinar By ComplianceOnline
Jul 2011
Clinical Document Management and Collaborative Electronic Data Exchange in Clinical Trials
Jul 2011
The Investigational Medicinal Product Dossier (IMPD): EU`s CTA vs. FDA`s IND
Jul 2011
Advertising and Promoting FDA Regulated Products - Webinar By ComplianceOnline
Jul 2011
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements
Jul 2011
How to Meet HIPAA-HITECH Encryption Requirements - Webinar By ComplianceOnline
Jul 2011
Using the USP Effectively - Webinar By ComplianceOnline
Jul 2011
Validation of Analytical Methods and Procedures - Webinar By ComplianceOnline
Jul 2011
Annual Clinical Trials Supply China
Jul 2011
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
Jun 2011
Navigating the new FDA world of Combination Products
Jun 2011
3hr Virtual Seminar on Designing Medical Devices for Patient Safety
Jun 2011
Designing an effective cleaning validation in today`s regulatory environment
Jun 2011
Sterilisation for Medical Devices
Jun 2011
Annual Global Pricing and Reimbursement for Med Device and Biopharmaceutical Manufacturers
Jun 2011
How to Survive a DEA Audit - Webinar By GlobalCompliancePanel
Jun 2011
Understanding good Closed Loop CAPA system - Webinar By GlobalCompliancePanel
Jun 2011
Medical Device Polymers
Jun 2011
Develop and Execute the Company Software V&V Program - Webinar By GlobalCompliancePanel
Jun 2011
Effective Risk Based Approach to Auditing and Qualifying Suppliers and Vendors - Webinar By GlobalCompliancePanel
Jun 2011
Risk-Based Validation for GxP Facilities - Webinar By GlobalCompliancePanel
Jun 2011
Sterilization Options for Challenging Products
May 2011
Pharmaceutical and Medical Device Validation Guidance`s - Similarities and Differences - Webinar By GlobalCompliancePanel
May 2011
`The Right Stuff` – Implementing Quality Control Tools in Quality Systems Operations
May 2011
BIT’s Annual World Congress of Cancer (WCC)
May 2011
Packaging and Labeling
May 2011
Medical Electronic Device Conference & Expo – MEDCon
May 2011
Imaging and Signal Processing in Healthcare and Technology - ISPHT
May 2011
Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
May 2011
Retirement of Computer Systems: Strategies for FDA Compliance and Tools for Implementation
May 2011
National Conference on the FCPA and Anti-Corruption for the Life Sciences Industry
May 2011
The GCP/ICH Obligations of Sponsors, Monitors, and Investigators - barriers and solution - Webinar By GlobalCompliancePanel
May 2011
CLEAN ROOMS - Standards & Technology
May 2011
KIHE
May 2011
ESEC
May 2011
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP
May 2011
Information Security Risk Analysis: Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePanel
May 2011
FDA`s New Enforcement of 21 CFR Part 11 - Webinar By GlobalCompliancePanel
May 2011
Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel
May 2011
Gowning Systems Used in Cleanrooms & Controlled Environments - Webinar By GlobalCompliancePanel
Apr 2011
Best Practices for the Implementation and Use of Test Management Tools - Webinar By GlobalCompliancePanel
Apr 2011
Establishing a Reduced Testing Program for Pharmaceutical & Medical Device Components
Apr 2011
Avoiding `Failure to Investigate` - Observations by Conducting Effective Investigations
Apr 2011
The FDA’s final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers
Apr 2011
How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel
Apr 2011
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements - ComplianceOnline Medical Device Training
Apr 2011
Process Validation for Medical Device Manufacturers
Apr 2011
Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel
Apr 2011
Preparing for Pre-approval Inspections - Webinar By GlobalCompliancePanel
Apr 2011
The 510(k) Process and Risk Management
Apr 2011
Data Security Analysis for Healthcare Providers - Webinar By GlobalCompliancePanel
Apr 2011
FDA`s Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List - Webinar By GlobalCompliancePanel
Apr 2011
Understanding Attribute Acceptance Sampling including Z1.4 and c=0 Plans - Webinar By GlobalCompliancePanel
Apr 2011
Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel
Apr 2011
Cloud Computer Training: Amazon Web Services for Science & Engineering Boston
Apr 2011
FDA`s Revised 510(k) Premarket Notification Process
Apr 2011
Decoding CLIA Regulations: Calibration, Calibration Verification and Method Validation
Apr 2011
Change Control -- Your Company`s GMP Weak Point - Webinar By GlobalCompliancePanel
Apr 2011
The Use and Mis-use of FMEA in Medical Device Risk Management - Webinar By GlobalCompliancePanel
Apr 2011
Controlled Substances and the Hospital Pharmacy - Webinar By GlobalCompliancePanel
Apr 2011
Cloud Computer Training: Amazon Web Services for Science & Engineering Bethesda
Apr 2011
ICD-10 Transition Guide & HCC Best Practices
Apr 2011
Clinical Trial Supply & Logistics World Asia
Mar 2011
Understanding the Calibration Curve - Webinar By GlobalCompliancePanel
Mar 2011
A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - Webinar By GCPanel
Mar 2011
The Pharmaceutical Quality System - Webinar By GlobalCompliancePanel
Mar 2011
Navigating the Regulatory Environment for the Implementation of Alternative Microbiology Technologies - Webinar By GCPanel
Mar 2011
International Dental Show (IDS)
Mar 2011
Rapid World
Mar 2011
Meet FDA Expectations for a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
Mar 2011
Annual Pricing & Reimbursement for Medical Devices
Mar 2011
Medical Device Recalls: How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel
Mar 2011
How to use QSIT to Your Advantage - Webinar By GlobalCompliancePanel
Mar 2011
Belgian Association of Pharmamaceutical Physicans Annual Scientific Conference & Provider Exhibition
Mar 2011
Annual Advances in Arthritis, Arthroplasty and Trauma Course
Mar 2011
Classification, Labelling and Packaging of mixtures and Substances
Mar 2011
Clinical Supply Chain Optimization
Mar 2011
Off-Label Promotion of Drugs - Regulatory Documents Explained - Webinar By GlobalCompliancePanel
Mar 2011
Cloud Computer Training: Amazon Web Services for Science & Engineering San Diego
Mar 2011
BIO-SAFETY AND BIO-SECURITY
Mar 2011
Process Validation: current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel
Mar 2011
MDD Exec - Sales and Marketing Excellence
Mar 2011
Recruiting is Critical to Your Success: What is the Secret - Webinar By GlobalCompliancePanel
Mar 2011
Project Management for Clinical Trials - Webinar By GlobalCompliancePanel
Mar 2011
Food Drug & Cosmetic Act: Implementing Regulations & Major New Laws - An Overview - Webinar By GlobalCompliancePanel
Mar 2011
Integrating a Quality Management System and Risk Management for Medical Devices Dallas
Mar 2011
The Investigation System (Discovery, Planning, Root Cause Analysis, CAPA) - Webinar By GlobalCompliancePanel
Mar 2011
IN-VITRO DIAGNOSTICS
Feb 2011
Middle East Conference on Biomedical Engineering (MECBME)
Feb 2011
BIOMEDevice Europe
Feb 2011
Why is CAPA so often cited in medical device inspections - Webinar By GlobalCompliancePanel
Feb 2011
Using Foreign Trial Data in Your NDA Approval Process - Webinar By GlobalCompliancePanel
Feb 2011
Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - Webinar By GlobalCompliancePanel
Feb 2011
Software Verification and Validation Planning and Execution
Feb 2011
International FORUM Medical Devices & Processes
Feb 2011
Electronic Raw Data in Regulated Environments - Definition, Recording and Archiving - Webinar By GobalCompliancePanel
Feb 2011
Structuring, Negotiating and Managing Life Sciences Collaborative Agreements and Acquisitions
Feb 2011
Medical Device Reporting Regulations and Violations - Webinar By GlobalCompliancePanel
Feb 2011
Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel
Feb 2011
Don`t RISK to ignore RISKS. Understanding ISO 14971
Feb 2011
Full Day Virtual Seminar : Process Validation for Medical Devices - FDA Inspectors are Checking – Are You Prepared?
Feb 2011
CE Marking: Obtaining and Maintaining EU Compliance Under the Medical Device Directive 2010
Feb 2011
DesignMed
Feb 2011
Pharma IP Innovations Forum
Feb 2011
Webinar on Medical Device Tracking
Feb 2011
Utilizing Good Requirements as a Foundation for the Effective Validation of PDMA-related Computerized Systems - Webinar By GlobalCompliancePanel
Feb 2011
Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel
Feb 2011
AN INTRODUCTION TO POST MARKETING SURVEILLANCE AND THE EUROPEAN MEDICALDEVICE VIGILANCE SYSTEM
Feb 2011
Analytical Instrument and Equipment Qualification in Quality Laboratories - Webinar By GlobalCompliancePanel
Feb 2011
Risk-Based Verification and Validation Planning to Meet U.S. FDA, ICH Q9 and ISO 14971
Feb 2011
Medical Device Patent Litigation
Feb 2011
Annual Scientific Advantage Medical Affairs & MSL Leadership Forum
Jan 2011
The Life Sciences Lawyer`s Guide to
Jan 2011
Medical Device Directive And Future Recast
Jan 2011
Webinar on Pharmacovigilance Audit - Webinar By GlobalCompliancePanel
Jan 2011
Medical Device Complaints Handling Strategies for Managing Your Biggest Compliance Challenge
Jan 2011
Global Medical Device Packaging and Labelling Compliance
Jan 2011
Assessing FDA’s Proposed Changes to the 510(k) Process in
Jan 2011
Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel
Jan 2011
Full day Virtual Seminar - Compliance for 21 CFR Part 11, reducing costs using risk-based computer system validation
Jan 2011
Understanding and Preparing for FDA`s New Part 11 Inspection Program - Webinar By GlobalCompliancePanel
Jan 2011
Anatomy of a Medical Device Inspection: From EIR to 483 to Warning Letter
Jan 2011
Clear as Mud: Obtaining and Marketing Your 510(k) With Today`s FDA San Francisco
Jan 2011
Clear as Mud: Obtaining and Marketing Your 510(k) With Today`s FDA Irvine
Jan 2011
Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel
Jan 2011
Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel
Jan 2011
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences - Part I and Part II - Webinar By GlobalCompliancePanel
Jan 2011
Social Media for Pharma
Jan 2011
101 cGMP To-Do List for - Webinar By GlobalCompliancePanel
Jan 2011
A Comparison of ICH Q-10 Quality System and the FDA`s Quality Systems Approach (QSA) to the Pharmaceutical GMPs - Webinar By GlobalCompliancePanel
Jan 2011
Solutions for addressing microbial excursions in medical device, pharmaceutical, and biotech industries
Jan 2011
Society of Electron Microscopy Technology Meeting (SEMT)
Dec 2010
Operational Excellence in Pharmaceuticals, Biotech and Medical Devices
Dec 2010
The FDA`s Working Group Reports, I & II - New Directions - Webinar By GlobalCompliancePanel
Dec 2010
Validating Excel and Word Applications Documents - ComplianceOnline Medical Device Training
Dec 2010
Recalls of Medical Devices in the US
Dec 2010
Medtech 10
Nov 2010
Updated EU filing and registration procedures (including the new variation rules coming in to force) - ComplianceOnline Medical Device Training
Nov 2010
EU Medical Device Changing Regulatory Landscape; Changes Now and What Current Re-writes Hold for 2011-12 - ComplianceOnline Medical Device Training
Nov 2010
How to Use Foreign Trial Data in Your NDA Approval Process
Nov 2010
Full Day Virtual Seminar - Reduce Software Validation Costs and Pass the New 21 CFR Part 11 Inspections - by GlobalCompliancePanel
Nov 2010
Pharmaceutical Packaging Leadership Summit
Nov 2010
Meeting the FDA: How to get the best advice from the FDA - ComplianceOnline FDA Training
Nov 2010
Pharma-Bio-Med
Nov 2010
Recent Advances in Microbial Control
Nov 2010
ISABEL - International Symposium of Applied Sciences in Biomedical and Communication Technologies
Nov 2010
Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process
Nov 2010
Shanghai International Traditional Medicine & Health Exhibition (The Session）
Nov 2010
SEBIO
Nov 2010
The IEEE International Conference on Information Technology and Applications in Biomedicine (ITAB)
Nov 2010
Columbia Business School Annual Healthcare Conference
Nov 2010
Annual SoCalBio Investor & Partnership Conference
Nov 2010
Medical Product Outsourcing Symposium (MPO)
Nov 2010
Q4 EMT (Emerging Medical Technologies) Spotlight
Nov 2010
Controlling Change to meet GMP Requirements
Nov 2010
Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs
Oct 2010
Full Day Virtual Seminar - Design and Validation of Excel Spreadsheets: Step-by-Step
Oct 2010
The Most Common Problems in FDA Software Validation & Verification - Webinar by GlobalCompliancePanel
Oct 2010
Validation Basics A-Z: Planning, Implementing & Maintaining
Oct 2010
ComplianceOnline Virtual Seminar - 21 Cfr Part 11: Complete Manual For Compliance Success
Oct 2010
Congress of Neurological Surgeons Annual Meeting
Oct 2010
International Symposium on MR-guided Focused Ultrasound
Oct 2010
The Tougher U.S. FDA - One Year Later
Oct 2010
The International Conference on Intelligent Information Hiding and Multimedia Signal Processing (IIHMSP)
Oct 2010
Phoenix
Oct 2010
ICMD
Oct 2010
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements in a Cost Effective Manner - Webinar by GlobalCompliancePanel
Oct 2010
Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective
Oct 2010
RFID in Health Care East
Oct 2010
What exactly is required for 21 CFR Part 11 compliance?
Oct 2010
Best Practices for Writing an Effective SOP to Lead to Successful FDA Inspections
Oct 2010
Integrating Clinical Evaluation and Risk Management (ISO 14971)
Oct 2010
Best Practices for Managing FDA Investigators and Handling FDA 483 Observations
Sep 2010
Development, Management, and Operation of an Effective Supplier and Internal Auditing System - Webinar by GlobalCompliancePanel
Sep 2010
Ensuring GCP compliance through quality auditing in clinical trial
Sep 2010
Robust Process Validation for Medical Devices - Webinar by GlobalCompliancePanel
Sep 2010
Validating Radiation Sterilization for medical device industries
Sep 2010
Understanding and Preparing for FDA`s New Part 11 Inspection Program
Sep 2010
Effective Quality Process Improvement for Medical Device Firms: Don’t get caught managing process through standardized SOP’s
Sep 2010
Compiling the Design History File, and Technical File / Design Dossier - Webinar by GlobalCompliancePanel
Sep 2010
The ICF Process: Tips on Achieving Optimal compliance and Comprehension
Sep 2010
Developing Supplier Quality Auditor Training Programs
Sep 2010
Medical Devices in the EU: CE Mark and 93/42/EEC Directive
Sep 2010
Developing an ethylene oxide (EO) sterilization process for a product with limitations
Sep 2010
Understanding Acceptance Activities for Medical Devices - Webinar by GlobalCompliancePanel
Sep 2010
Astana Zdorovie - International Kazakhstan Exhibition on Healthcare
Sep 2010
Effective & Essential CAPA process to avoid FDA 483 - Webinar by GlobalCompliancePanel
Sep 2010
Key Modules of an Effective CAPA SOP - Webinar by GlobalCompliancePanel
Sep 2010
Post-Design Medical Device Risk Management - Webinar by GlobalCompliancePanel
Sep 2010
Understanding Corrective and Preventive Action, and Elements of a CAPA System - Webinar by GlobalCompliancePanel
Sep 2010
Product Risk Management - ISO 14971 and ICH Q9
Aug 2010
Conducting Value Added Audits of Technical Service Providers - Webinar by GlobalCompliancepanel
Aug 2010
Understanding International Standards for Medical Devices
Aug 2010
Regulatory Requirements for Medical Device Calibration Programs - Webinar by GlobalCompliancepanel
Aug 2010
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements - Webinar by GlobalCompliancepanel
Aug 2010
Important Sterilization Information for Product Developers - Webinar by GlobalCompliancePanel
Aug 2010
Failure Modes and Effects Analysis (FMEA) - An Effective Tool for Medical Device Risk Management - Webinar by GlobalCompliancePanel
Aug 2010
CMEF Regional
Jul 2010
Medical Device Chief Marketing Officer Summit
Jun 2010
Medical Device Pricing & Reimbursement
Jun 2010
Scandinavian Medical Technology Conference
May 2010
Pragomedica
Apr 2010
Meditec Clinika
Feb 2010
An Introduction To Post Marketing Surveillance And The European Medical Device Vigilance System
Feb 2010
Facility And Equipment Verification
Feb 2010
Revision To The Medical Device Directives
Feb 2010
CALIBRATION - The Risk Based Approach to Calibration Management
Jan 2010
US FDA Quality Systems & Medical Device Requirements
Dec 2009

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Global Women in Leadership summit {US Edition}
New York City
29-30 May 2025
The Learning Ideas Conference 2025

The Learning Ideas Conference 2025
New York City
11-13 Jun 2025
AI World Congress 2025

AI World Congress 2025
London
18-19 Jun 2025
EDULEARN 25 - The 17th annual International Conference on Education and New Learning Technologies

EDULEARN 25 - The 17th annual International Conference on Education and New Learning Technologies
Palma
30 Jun - 02 Jul, 2025
International Conference on Trends and Innovations in Management, Engineering, Sciences and Humanities (ICTIMESH 2025)

International Conference on Trends and Innovations in Management, Engineering, Sciences and Humanities (ICTIMESH 2025)
London
30 Jun - 03 Jul, 2025
International Conference on Engineering, Economics, Management, and Applied Sciences (ICE2MAS 2025)

International Conference on Engineering, Economics, Management, and Applied Sciences (ICE2MAS 2025)
Bangkok
07-10 Jul 2025
Primary Care Hawaii Conference - Caring for the Active and Athletic Patient

Primary Care Hawaii Conference - Caring for the Active and Athletic Patient
Koloa
21-25 Jul 2025
International Conference on Communication, Business and Technology (Including Ai)

International Conference on Communication, Business and Technology (Including Ai)
Accra
18-20 Aug 2025
International Conference on Culture, Languages and Linguistics

International Conference on Culture, Languages and Linguistics
Accra
20-22 Aug 2025
International Conference on African Studies and Theatre Arts

International Conference on African Studies and Theatre Arts
Accra
25-27 Aug 2025
International Conference on African Tourism and Hospitality Management

International Conference on African Tourism and Hospitality Management
Kigali
01-03 Oct 2025
International Conference on Interdisciplinary Studies

International Conference on Interdisciplinary Studies
Kigali
06-08 Oct 2025
International Conference on Health, Science and Technology

International Conference on Health, Science and Technology
Kigali
08-10 Oct 2025
International Conference on Global Tourism and Hospitality Management

International Conference on Global Tourism and Hospitality Management
Marsa
11-13 Nov 2025
Global Management Conference and Workshop

Global Management Conference and Workshop
Manchester
26-28 Nov 2025

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