Conferences on Medical laboratories (past events)

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International Pharma Congress
Nov 2024
Meeting of the Royal Belgian Society for Laboratory Medicine (RBSLM)
Nov 2024
World Companion Diagnostics and Liquid Biopsy Summit APAC
Nov 2024
International Vaccine Congress (IVC)
Nov 2024
Next Generation Pharmaceutical Cleanroom
Oct 2024
AstanaZdorovie
Oct 2024
LIFE - Laboratory Insights for Excellence
Oct 2024
International Conference on Clinical and Experimental Cardiology Research
Sep 2024
International Conference on Telemedicine and Digital Health
Sep 2024
Aseptic Processing Technology
Sep 2024
Global Conference on Medical and Health Science (GCMHS)
Sep 2024
International Conference on Traditional and Alternative Medicine
Aug 2024
Global Pharmacovigilance & Clinical Trials Summit
Jul 2024
Pharma Anti Counterfeiting & Serialisation
Jun 2024
International Conference on Pharmaceutical Formulations and API
May 2024
Highly Potent Active Pharmaceutical Ingredients
May 2024
Lab Ops and Facility Management for Biopharma Summit
May 2024
China Consumer Health Digital Innovation Summit
May 2024
MEDEXPO Africa
Apr 2024
International Congress - EBART (Evidence Based Assisted Reproductive Technologies)
Apr 2024
International Conference on Immunity and Immunochemistry
Mar 2024
Clinical Trial Billing and Research Compliance Summit
Mar 2024
International Precision Med TRI-CON
Mar 2024
Odisha Medical Expo
Feb 2024
Conference on Laboratory Medicine & Pathology
Dec 2023
International Conference on Neurology and Neuro Disorders
Dec 2023
Bio-IT World Europe Conference & Expo
Nov 2023
International Conference on Structural Biology and Mass Spectrometry
Nov 2023
Ophthalmic Drugs
Nov 2023
European Conference on Advance Clinical Trials and Research
Nov 2023
ADSCC Bone Marrow Transplant & Cellular Therapy Congress
Nov 2023
Next Generation Gene Therapeutics
Nov 2023
International Specialized Exhibition Clean Rooms Technologies CleanTechExpo
Oct 2023
International Conference on Polymer Chemistry
Oct 2023
International Medical Exhibition - Public Health
Oct 2023
International Virtual Conference on Nursing Research, Patient Safety and Healthcare
Oct 2023
iMED Medical Equipment Exhibition (iMed)
Oct 2023
MarketsandMarkets Next-Gen Digital Pathology Conference
Oct 2023
Evaluating Biopharma: Continuous Bioprocessing
Oct 2023
International Conference on Oncology and Cancer Research
Oct 2023
International Conference on Biomarkers and Cell Biology
Sep 2023
International Conference on Clinical Trials
Sep 2023
Philippines Laboratory Expo
Aug 2023
Global Summit on Cardiology & Emergency Medicine
Aug 2023
Sri Lanka Medical Association (SLMA) International Medical Congress
Jul 2023
PDA Cell and Gene Pharmaceutical Products Conference
Jul 2023
International Conference on Clinical Research
May 2023
Clinical Autonomic Disorders: Case-Based and Laboratory Workshop
May 2023
PEGS Boston Conference & Expo
May 2023
Good Laboratory Practice & Good Clinical Laboratory Practice
May 2023
Quality Control Laboratory Compliance - cGMPs and GLPs
Apr 2023
International Meeting & Exhibition on Medicinal Chemistry and Pharmaceutical Science
Mar 2023
World Congress on Primary Healthcare and Medicare Summit
Feb 2023
Life Sciences, Clinical Trials, Patient Recruitment & Retention
Jan 2023
Evaluating Biopharma - Cell Therapy Strategies
Dec 2022
World Conference and Exhibition on Forensic Science
Nov 2022
Early & Managed Access Programmes
Nov 2022
CHEM-LAB-ANALYT
Oct 2022
Accelerating Clinical Trials in Asia
Oct 2022
HPAPI Handling & Manufacturing Summit
Sep 2022
Clinical Project Management MasterClass
Sep 2022
World Congress On Pathology, Microbiology & Clinical Practice
Sep 2022
International Conference on Healthcare Engineering (ICHE)
Sep 2022
World Congress on Pathology and Microbiology
Sep 2022
Integrin-Targeted Drug Development Summit
Sep 2022
Pharma Summit : Drug Discovery & Community Trial
Aug 2022
Operationalize: Electronic Trial Master Files
Aug 2022
Global Experts Meeting on Pathology and Laboratory Medicine
Jul 2022
WYN Cardiology Forum
Jul 2022
Analytical Instrument Qualification & Validation - Use of Excel and FDA Audit Preparation
Jul 2022
How to Apply for a Breakthrough Therapy Designation and Win It
Jun 2022
Medical Device Regulations & Compliance Summit
May 2022
Pharmacokinetics (PK) / Pharmacodynamics (PD) Studies in Drug Discovery and Development
May 2022
Packaging and Labeling in Pharmaceutical Product Development - Best Practices
May 2022
MedTech Korea Summit
Apr 2022
International Conference on Clinical Chemistry and Laboratory Medicine
Mar 2022
Scholars International Webinar on Advances in Drug Discovery and Development
Mar 2022
Contemporary Challenges in Bioethics and Clinical Research : AI, Big Data, and Privacy
Mar 2022
3-Hour Virtual Seminar on IQ, OQ, PQ in the Verification and Validation Process
Mar 2022
Regulated LC-MS Bioanalysis Masterclass
Jan 2022
UCG on Diabetes and Endocrinology Conference
Jan 2022
Annual Assoc. for Mass Spectrometry: Applications to the Clinical Lab (MSACL US)
Dec 2021
PHARMAC India
Dec 2021
Clinical Trial Innovation Summit
Dec 2021
Cleaning Validation for Pharma
Dec 2021
Vendor/CRO Management and Oversight MasterClass
Nov 2021
ICBE : International Conference on Biomedical Engineering
Oct 2021
European Congress on Clinical trials and Clinical Research
Oct 2021
Medical Devices Innovation Programme
Oct 2021
Webinar: Harnessing the Power of Bispecific Antibodies
Oct 2021
Pharmacovigilance Aspects of Licensing Agreements
Oct 2021
Data Integrity: FDA/EU Requirements and Implementation
Sep 2021
International Conference on Environmental Indicators
Sep 2021
International Conference on Digital Pathology
Sep 2021
Investigator Initiated Trials
Sep 2021
Healthcare Planning & Infrastructure Expo (HPIE)
Sep 2021
Patient Recruitment, Engagement and Support Summit
Aug 2021
Risk Management in Medical Devices Industry
Jun 2021
AABB Meeting Highlights Conference and Exhibition in the Middle East
Jun 2021
Bangladesh Medical & Healthcare Virtual Expo
Jun 2021
Clinical Trials Inspection Readiness Summit
May 2021
Clinical Trials Innovation Programme
May 2021
Risk-Based Validation of Laboratory Computerised Systems MasterClass
May 2021
ProcureCon Pharma
May 2021
Middle East Laboratory and Diagnostics Congress
Apr 2021
Clinical Trials V-Forum
Apr 2021
Risk Management in Clinical Research
Mar 2021
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Mar 2021
Virtual On-line Conference on Clinical Trials & Clinical Research
Mar 2021
International Conference on Clinical Trials
Feb 2021
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
Plenareno Pharma Middle East Congress
Dec 2020
Annual Immune Checkpoint Inhibitors (ICI Europe)
Nov 2020
International Conference on Biologics and Biosimilars
Oct 2020
Optimizing Clinical Trials Summit: Site Selection, Feasibility & Patient Recruitment
Oct 2020
AAPS PHARMSCI 360 - The American Association of Pharmaceutical Scientists Meeting and Exposition
Oct 2020
European Pathology Congress and Expo
Oct 2020
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering Training
Oct 2020
Laboratory Inspection and Auditing
Oct 2020
Precision in Medical Devices Boston
Oct 2020
Precision in Drug Discovery & Preclinical Summit Boston
Oct 2020
Azerbaijan International Medical Innovations Exhibition (Medinex)
Oct 2020
Design of Experiments for Chemists and Engineers
Oct 2020
Digital Clinical Biomarkers and World CDx Summit
Oct 2020
AI-ML Clinical Development
Sep 2020
Biobanking
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
Product Selection & Pipeline Optimization for Generics
Sep 2020
International Conference on Pharmacoepidemiology and Clinical Research
Sep 2020
International Congress on Laboratory Medicine
Sep 2020
World Congress on Stem Cell and Regenerative Medicine
Sep 2020
World Congress on Advanced Clinical Research and Biomarkers
Sep 2020
Disclosure and Transparency for Clinical Data Summit
Aug 2020
International Conference on Medical and Health Science
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
Annual Global Healthcare Conference (GHC)
Jul 2020
Clinical Regulatory Medical Writing Forum
Jul 2020
International Conference on Laboratory Medicine and Mass Spectrometry (LMMS)
Jul 2020
International Conference On Medical and Nursing Education
Jul 2020
Precision in Clinical Trials Boston
Jul 2020
Medicinal Chemistry
Jun 2020
Transforming the face of Dentistry (IDF)
Jun 2020
Issues in Calibrations and Accuracy in Method Validation
Jun 2020
How to be Efficient and Compliant with Part 11, Validation, and SaaS/Cloud
May 2020
World Medical Nanotechnology Congress and Expo
May 2020
Digital Quality in Clinical Trials
May 2020
Digi-Tech Pharma & AI conference
May 2020
Predictive Analytics World Healthcare
May 2020
Environmental and Public Health Microbiology Conference
May 2020
Biomolecular Condensates Summit
Apr 2020
Global Congress and Expo on Medical imaging and Case reports
Apr 2020
eyeforpharma Medical Affairs USA
Apr 2020
International Conference on Integrated Medical Science and Allied Health (ICIMSAH)
Apr 2020
Adaptive Clinical Trials Symposium
Mar 2020
Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency
Mar 2020
Product Complaints Forum
Mar 2020
Pre-Filled Syringes
Mar 2020
Validation and 21 CFR Part 11 Compliance of Computer Systems
Feb 2020
Medexpo Africa (Ethiopia)
Feb 2020
T3: Trials, Tech and Transformation
Jan 2020
The A to Z`s of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems
Jan 2020
Laboratory medicine conference
Jan 2020
International Conference on Biochemistry & Biophysics
Dec 2019
Regulatory Requirements and Principles for Cleaning Validation
Dec 2019
Annual Global BioProduction Summit
Dec 2019
Clinical Microbiology Conference
Dec 2019
HR Life Sciences
Dec 2019
Virtual Clinical Trials Conference
Dec 2019
International Conference on Parasitology & Microbes
Dec 2019
Joint MHRA/DIA Excellence in Pharmacovigilance
Nov 2019
Biostatistics for the Non-Statistician
Nov 2019
MedHealth International trade exhibition - Kenya
Nov 2019
Scholars International Conference on Advances in Neurology and Neuropsychiatry
Nov 2019
Investigator-Initiated Trials (IIT) Forum
Nov 2019
Pharmaceutical Sciences And Drug Delivery
Nov 2019
Confidentiality of Substance Use Disorder Patient Records; Complying with the New Federal Law 42 CFR Part 2
Nov 2019
Annual Drug Discovery USA Congress
Oct 2019
FDA Scrutiny of Promotion and Advertising Practices
Oct 2019
Biennial Conference of Nuclear Cardiology Society of India
Oct 2019
Strategic Partnerships for Drug Repurposing Forum
Oct 2019
Global Staunch Congress on Health Care & Laboratory Medicine
Oct 2019
International Biochemistry Conference
Oct 2019
Saudi International Laboratory and Diagnostics Congress
Oct 2019
International Conference on Neonatology & Perinatology
Oct 2019
International Conference on Clinical Trials and Clinical Research
Oct 2019
Highly Potent Active Pharmaceutical Ingredients Summit
Oct 2019
International Research Conference on Science, Health and Medicine (IRCSHM)
Sep 2019
International Conference on Clinical Trials & Pharmacovigilance
Sep 2019
SmartLabs & Laboratory Informatics Congress
Sep 2019
Health Asia International Exhibition & Conference
Sep 2019
Stability Testing Summit
Sep 2019
World Congress: Delivering Therapies to the Clinic Faster
Sep 2019
Medical Devices Meetings Twente
Sep 2019
Clinical Trial Regulations With ICH GCP E6 R2 Workshop
Sep 2019
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
Sep 2019
Identify and Manage Data Integrity Issues, CSV and 21 CFR Part 11
Sep 2019
World Congress on Clinical Research and Biomarkers
Sep 2019
Clinical Research and Clinical Trials Summit
Sep 2019
American Society of Clincial Pathology (ASCP) Annual Meeting
Sep 2019
Implementing UDI (Unique Device Identification) - Plan Now for Success
Sep 2019
Cleanroom Design & Engineering Forum
Sep 2019
GMP Compliance for Quality Control and Contract Laboratories
Aug 2019
Trial Master File (TMF) Institute - Philadelphia
Aug 2019
Effective Supplier Management Programs
Aug 2019
21 CFR Part 11 and Risk Assessment
Jul 2019
Biosafety and Blood borne Pathogen Safety in the Lab
Jul 2019
6-Hour Virtual Seminar on Adaptive Design for Clinical Trials
Jul 2019
Auditing Laboratory Data Systems
Jul 2019
Basics of Testing Associated with Sterilization Validation and Routine Processing
Jul 2019
Establishing Appropriate Quality Metrics and Key Performance Indicators (KPIs)
Jul 2019
analytica Lab Africa
Jul 2019
International Conference on Clinical Research and Biomarkers
Jul 2019
Biocompatibility Testing for Medical Devices
Jun 2019
CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations
Jun 2019
International Conference on Biomedical and Clinical Research
Jun 2019
Demystifying the Canadian Drug and Health Products Regulatory Landscape
Jun 2019
The Great Plains Laboratory Presents GPL Academy Practitioner Workshops Minneapolis
Jun 2019
Auditing Laboratories Conducting Assays Supporting Biologics
Jun 2019
Power Analysis for Sample Size Calculations
Jun 2019
Onboarding: From Entry-Level to Senior Executive
Jun 2019
How to Prepare Yourself for FDA`s on-going Part 11 Inspection Program
Jun 2019
Solving Statistical Mysteries – What does the FDA want
Jun 2019
International conference on Pharmaceutical Chemistry & Drug Discovery
Jun 2019
CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process
Jun 2019
Project Management for Non-Project Managers
Jun 2019
BioMedical Sensors & Connected Devices Summit
Jun 2019
Implementing a Compliant Stability Program for Biologics
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
3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries
May 2019
The International Congress on Clinical Trials for Medical Devices (CTMD)
May 2019
New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines
May 2019
Documentation of Medical Necessity - Focus for OIG and other auditors
May 2019
Pharmaceutical Water Systems - Validation, Monitoring and Inspection Preparation
May 2019
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
May 2019
Analytical Techniques
May 2019
Stability Studies & Estimating Shelf Life
May 2019
Quality Control for Microbiological Media and Reagents
May 2019
Compliance Measures for Case Managers
May 2019
GMP Environmental Monitoring in Pharmaceutical Clean Rooms
May 2019
The Great Plains Laboratory Presents GPL Academy Practitioner Workshops San Francisco
Apr 2019
Ensuring your Site is Ready for an FDA Inspection
Apr 2019
Risk Management in Clinical Research
Apr 2019
World Conference on Bacteriology and Infectious Diseases
Apr 2019
3-Hour Virtual Seminar on Safety Audits and Pharmacovigilance (PV) Inspections
Apr 2019
International Conference on Laser, Optics and Photonics
Apr 2019
Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA
Apr 2019
Analytical Method Validation and Transfer
Apr 2019
Compliance with the New ICH GCP Revision 2 Addendum
Apr 2019
Biosimilars and Follow-On Biologics Americas
Mar 2019
The International event for the Life Science and Technology Industries (LSIE)
Mar 2019
Method Development and Validation for Assays Supporting Testing of Biologics
Mar 2019
QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and Transfer
Mar 2019
BIHE Healthcare & Dental Exhibition (Cancelled)
Mar 2019
FDA Inspections - Do`s and Don`ts
Mar 2019
Global Experts Meeting on Frontiers in Nanomedicine and Drug Delivery
Mar 2019
How to apply ISO 62304 standard in a medical software development project?
Mar 2019
Trial Master File Institute - Frankfurt
Mar 2019
Theory and Practice of Near-Infrared Spectroscopy
Mar 2019
FDA`s Quality Metrics - Latest Advances
Mar 2019
eyeforpharma Medical Affairs Europe
Mar 2019
Sterilization Processes - The Methods, Parameters and Deficiencies
Mar 2019
How to Implement a Quality Management System According ISO 13485?
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
Pediatric Clinical Trials Conference
Mar 2019
World Congress on Pathology and Laboratory Medicine
Feb 2019
Immunotherapeutics & Immunomonitoring Conference
Feb 2019
The New ICH GCP E6 R2 Guideline
Feb 2019
annual DPharm Europe: Disruptive Innovations to Advance Clinical Trials
Feb 2019
Euroscicon Conference on Biosimilars
Feb 2019
Is it Method Verification or Validation, or Just Semantics
Feb 2019
International Conference on Artificial Intelligence, Soft Computing and Applications (ICA2SC)
Feb 2019
Analytical Method Transfer According to USP General Chapter-1224
Feb 2019
World Congress on Drug Discovery and Drug Design
Feb 2019
Measurement Systems Analysis
Feb 2019
International conference on Biomarkers and Cancer Targets
Feb 2019
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
Feb 2019
The Great Plains Laboratory GPL Academy Practitioner Workshops
Feb 2019
China & Pacific Rim Markets: Compliance Processes for Life Science Products - Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations
Jan 2019
Tips and Techniques for Handling Missing Data (Statistical Techniques)
Jan 2019
Data Governance for Computer Systems Regulated by FDA
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
Sample Size Determination for Design Validation Activities
Dec 2018
Annual Healthscape Summit
Dec 2018
Handling Situations Where Regulation E and ACH Don`t Align
Dec 2018
FDA Regulations for Analytical Instrument Qualification and Validation – Comprehensive Best Practices
Dec 2018
Seasonal Influenza Vaccines- Current Concepts and Future Trends for Effective Immunization
Dec 2018
Medical Devices - ISO 13485
Dec 2018
TMF Plus and eCTD Plus
Dec 2018
Is your Medical Device Software 510(k) Ready?
Dec 2018
Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
Dec 2018
Edition of EuroScicon Conference on Advanced Stem Cells & Regenerative Medicine
Dec 2018
Quality Control for Analytical Materials used in Microbiology Laboratories
Dec 2018
World Biobanking Summit
Nov 2018
International Conference on Virology, Bacteriology & Infectious Diseases
Nov 2018
Global Pre-Filled Syringes Summit
Nov 2018
Excel Formulas and Functions
Nov 2018
MedChem
Nov 2018
Asia-Pacific Conference on Intelligent Medical (APCIM)
Nov 2018
Qualification and Validation of Laboratory Equipment and Systems for Regulated Industries
Nov 2018
International Conference on Generic Drugs and Biosimilars
Nov 2018
Control-Analysis Instrumentation used in PAT Continuous Manufacturing
Nov 2018
Auditing for Microbiological Aspects in Pharmaceutical Manufacturing
Nov 2018
Process Verification and Validation
Nov 2018
How to Write SOPs which are Compliant for Inspections for a GXP Compliance
Nov 2018
Good Documentation and Record Keeping Best Practices (FDA & EMA)
Nov 2018
Bioequivalence, Dissolution & IVIVC Training
Nov 2018
Ensuring Integrity and Security of Laboratory Data
Nov 2018
Annual congress on Medicine
Nov 2018
International Kidney Cancer Symposium
Nov 2018
Astana Zdorovie
Nov 2018
International Conference on Forensic Research & Forensic Chemistry
Nov 2018
Annual High Potent Medicines Conference
Oct 2018
Requirements for IQ, OQ and PQ Quality Protocols
Oct 2018
EM-PHASES
Oct 2018
HR Life Sciences
Oct 2018
Sterilization of Pharmaceutical Products and Medical Devices
Oct 2018
International Conference on Decontamination, Sterilization and Infection Control
Oct 2018
Aseptic Process Overview and Validation
Oct 2018
International Conference on Molecular Markers and Cancer Therapeutics
Oct 2018
Annual Biomarkers - CDx - Precision Immunotherapy Summit
Oct 2018
Troubleshooting Ethylene Oxide (EO) Processes
Oct 2018
Powerful Closed-loop CAPA - Meeting FDA Expectations
Oct 2018
Cleaning Validation Workshop
Sep 2018
Safety and Selectivity in the Scale-Up of Chemical Reactions
Sep 2018
International Colloquium on Medical & Clinical Trials
Sep 2018
FDA`s New Enforcement of 21 CFR Part 11
Sep 2018
Changes under the HIPAA Omnibus Rule - What`s New
Sep 2018
Leveraging the Laboratory : The Power of Outreach
Sep 2018
Gut Health Congress Asia
Sep 2018
International Conference on Clinical Pharmacy and Public Health
Sep 2018
Annual Clinical Trials Quality & Compliance
Sep 2018
cGMPs in the Quality Control Laboratory
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
CGMP controlled Raw Materials
Sep 2018
Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success
Sep 2018
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Sep 2018
Medical Tubing
Sep 2018
International Conference on World HPLC & Separation Techniques
Aug 2018
Pharmaceutical Validation - Latest Global Regulations and Trends to Stay Compliant
Aug 2018
PREDiCT:3D Models Summit
Aug 2018
Global Experts Meeting on Clinical Research and Clinical Trials
Aug 2018
Global Pharmaceutical & Clinical Research Summit
Aug 2018
CMS Hospital CoP and TJC Telemedicine Standards, Telemedicine Credentialing and Privileging
Jul 2018
Opioid Abuse in the Workplace: Using Effective Drug Testing and Policies to Reduce the Pain of the Painkiller Epidemic
Jul 2018
Laboratory Investigations for Out of Specification Results
Jul 2018
New Revision of USP <1058>: Analytical Instrument Qualification
Jul 2018
World Drug Delivery and Novel Therapy Summit
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
Annual Conference on Clinical Research & Biomarkers
Jul 2018
Root Cause Analysis (RCA) in the Laboratory - Addressing Non-Conformances
Jul 2018
Good Documentation Guideline (Chapter <1029> USP)
Jul 2018
Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals
Jul 2018
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay that Way
Jul 2018
Deviation Investigation Best Practices: Ensuring Correct Content and Conclusions
Jul 2018
Patients Suing Under HIPAA
Jul 2018
Develop a Compliant Validation Protocol and Analytical Procedures according to the FDA Guidance and USP Good Documentation Practices
Jul 2018
World Conference on Parasitology
Jul 2018
Product Information for Medicinal Products in the EU
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
Additive Manufacturing Europe
Jun 2018
Water System Investigation `How-To`s` and Example Case Studies
Jun 2018
Biocompatibility Testing; what you need to know
Jun 2018
Food Fraud in the Organic Industry
Jun 2018
Oversight of CROs-Vendors-CMOs
Jun 2018
Off label Promotion of Drugs and Medical Devices - FDA`s Latest
Jun 2018
International Conference on Science, Management, Engineering and Technology (ICSMET)
Jun 2018
Pharmaceutical Logistics
May 2018
Annual Conference on Stability Program
May 2018
Does your QC lab do GMP and non-GMP activities?
May 2018
Why and How - Verification of Compendial Methods - USP [1226]
May 2018
World Liver Conference
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
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
Fundamentals of Risk Management in Clinical Research
May 2018
Auditing Analytical Laboratories for FDA Compliance
May 2018
How to Comply with 21 CFR 11 Requirements for Electronic Medical Records
May 2018
Failure Modes and Effects Analysis
Apr 2018
mHealth for Clinical Trials EU
Apr 2018
Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities
Apr 2018
Kuwait Medica Conference & Exhibition
Apr 2018
International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems
Apr 2018
Clinical Trial Collaborations
Apr 2018
Differences Between ISO 13485 & ISO 9001 - and How to Choose Which One to Implement
Apr 2018
International Conference & Exhibition on Biologics and Biosimilars
Mar 2018
LabtechMED Eurasia
Mar 2018
AACC Middle East
Mar 2018
TMF Operations: a Quality and Regulatory Approach
Mar 2018
annual Conference on Pediatric Clinical Trials
Mar 2018
Cannabis Partnerships Congress
Mar 2018
Global CDx & Personalized Medicine Summit
Mar 2018
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program
Mar 2018
Cell culture Downstream world Congress
Feb 2018
Ensuring Data Integrity in Method Validations
Feb 2018
Cleanroom Technology Summit and Exhibition
Feb 2018
GMP for Quality Control Laboratories and FDA Audit Preparation
Feb 2018
A Risk Based Approach To Data Integrity
Feb 2018
GPL University Practitioner Workshops
Feb 2018
Drug Dissolution Testing and Establishing Plasma Drug Levels in Humans
Feb 2018
Medlab ME
Feb 2018
Synthetic Lethality Conference
Feb 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
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
International Conference on Healthcare and Biological Research (ICHBR)
Dec 2017
Med- tech Summit
Dec 2017
Dubai International Laboratory and Diagnostics Congress
Dec 2017
Data Integrity and Protection for Clinical Research Summit
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
Why you Should be Worried about HIPAA
Dec 2017
Laboratory Informatics Summit
Dec 2017
Adverse Events Reporting and Safety Strategies Summit
Dec 2017
Why are we Seeing More Independent Data Safety Monitoring
Dec 2017
Analytical Method Validation Under Good Laboratory Practices - GLPs
Dec 2017
Lab Automation & Robotics
Nov 2017
Annual COPD: Novel Therapeutics and Management Strategies
Nov 2017
Dealing with Performance Issues
Nov 2017
Human Subjects Research Seminar: Current Regulations under FDA and HIPAA
Nov 2017
GMP Compliance for Quality Control and Contract Laboratories
Nov 2017
Auditing Analytical Laboratories for FDA Compliance
Nov 2017
Women in Pharma and Medical Leadership Summit
Nov 2017
Digital Pathology Congress
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
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Nov 2017
Global Nursing and Healthcare Summit
Nov 2017
Statistics for the Non-Statistician
Nov 2017
Statistical Methods A Visual Approach
Nov 2017
Antibodies and Bio Therapeutics Congress
Nov 2017
Medical Device Hazard Analysis Following ISO 14971
Nov 2017
World Congress on Pharma and Advanced Clinical Research (Pharmacon)
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
World Congress on Embryology and In vitro Fertilization
Nov 2017
Virtual Seminar on Analytical Method Validation Process
Nov 2017
Annual Clinical Forum and Exhibition
Oct 2017
World Clinical Medicine & Collaboration Forums
Oct 2017
Annual Partnerships in Clinical Trials US
Oct 2017
Bioequivalence Summit
Oct 2017
Annual Biorepositories and Sample Management Summit
Oct 2017
International Conference on Biomarkers
Oct 2017
Annual Companion Diagnostics (CDx) Summit Oncology & Beyond: Clinical Applications, Regulation, & Reimbursement
Oct 2017
Neglected Tropical Diseases Forum
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
DMC Optimization Summit
Oct 2017
ICEIAM : International Conference on Environmental, Industrial and Applied Microbiology
Oct 2017
The Annual Personalized & Precision Medicine Conference
Oct 2017
FDA Regulations for Analytical Instrument Qualification and Validation Processes
Oct 2017
International Conference on Biomedical Engineering (ICBE)
Oct 2017
Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes
Oct 2017
Annual Single Cell Analysis Asia Congress
Oct 2017
Laboratory Instrument Calibration
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
Excellence in Pharmacovigilance: Clinical Trials and Post-Marketing
Oct 2017
GLP Quality System Essences and Comparison with GMP
Oct 2017
Point of Care Testing Advances Conference Abu Dhabi
Sep 2017
Annual Pre-Filled Syringes Summit
Sep 2017
NCCR - National Conference for Clinical Research
Sep 2017
Combination Products
Sep 2017
FierceBiotech Drug Development Forum
Sep 2017
Annual Cancer Immunotherapy Summit
Sep 2017
Writing and implementing effective SOP`s
Sep 2017
ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices
Sep 2017
Microbiome AgBioTech Europe Summit
Sep 2017
Effective Training Practices for FDA Compliance
Sep 2017
Document Control and Training
Sep 2017
VSICON
Sep 2017
MEDLAB Europe
Sep 2017
Modern Vaccines Adjuvants and Delivery Systems (MVADS)
Sep 2017
Best Practices for an Effective Cleaning Validation Procedures
Sep 2017
International Conference on Clinical Trials
Sep 2017
Investigation of Out-Of-Specification Laboratory Results
Sep 2017
2018 ICD-10-CM Update for Cardiology
Sep 2017
New Relationship between the Data Controller, Data Processor and the Data Subject
Sep 2017
International Meeting on Medicinal Plants and Natural Products Research
Sep 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
World Medical Laboratory Congress & Expo
Aug 2017
The Challenges of an Effective Change Control Program and How to Address OOS Results
Aug 2017
Documenting Software for FDA Submissions
Aug 2017
FDA Regulations for Environmental Monitoring (EM) Program
Aug 2017
Laboratory-Developed Tests: Why does FDA think they can Regulate them, and why do others think they Cannot
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
Building a Validation Program From Top to Bottom
Aug 2017
Biosimilar from Development to Registration
Aug 2017
Rare Disease Collaboration Summit
Jul 2017
AI Pharma Innovation
Jul 2017
NGS and Clinical Applications Congress: USA
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
Laboratory Accreditation: Getting there is just the beginning
Jul 2017
Trial Protocol Optimization and Design Congress
Jul 2017
Personnel Training to Assure FDA and ISO Compliance
Jul 2017
GLP Master Practitioner Workshop
Jul 2017
Supplier Management for Medical Device Manufacturers
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
Annual Vaccines + Therapeutics Summit
Jun 2017
Proton Therapy USA
Jun 2017
How To Establish an Effective Chief Compliance Officer`s (CCO) or Chief Risk Officer`s (CRO) Function - Organization and Responsibilities
Jun 2017
Laboratory, Medical and Device Performance and Validation following Regulatory and ICH Statistical Guidelines
Jun 2017
HPAPIs SUMMIT
Jun 2017
Animal Welfare Innovation Forum
Jun 2017
Complaints, Servicing and FDA Reporting
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
Improving Process Stability and Capability - Tips, Traps and Guidance
Jun 2017
World Biobanking Lisbon Summits
Jun 2017
Compliance with ICH GCP R2 Addendum for Auditors
Jun 2017
Steam Sterilization Microbiology and Autoclave Performance
Jun 2017
FDA Policy and Goals Regarding the 483 Response
Jun 2017
World Adoptive T-Cell Therapy Summit
May 2017
Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)
May 2017
FDA`s Expedited Development and Approval Programs: Taking the Mystery out of Expedited Approvals
May 2017
Radiation Sterilization of Medical Products - Beyond the Basics
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
New FDA or EMA and USP Guidelines for Transfer of Analytical Methods
May 2017
CRISPR Summit
May 2017
Phase I GMPs
May 2017
FDA`s GMP Expectations for Phase I and -in-Man Clinical Trials
May 2017
Extractables & Leachables USA
May 2017
Laboratory, Medical and Device Performance and Validation following Regulatory
May 2017
IPhEB & CPhi Russia
Apr 2017
Apteka Expo
Apr 2017
GxP (GMP, GLP, GDP) Data Integrity, Quality Metrics and FDA Inspections
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
PMBA - Project Management Business Administration
Apr 2017
Computer Systems Validation (CSV), Data Integrity, 21 CFR Part 11 Compliance and GAMP 5
Apr 2017
Next Generation Sequencing (NGS) Cyprus
Apr 2017
Medical Necessity: Can you define it, Capture it, Document it
Apr 2017
Tissue Engineering, Biofabrication & 3D-Bioprinting in Life sciences
Mar 2017
analytica Vietnam
Mar 2017
Annual Pharmaceutical Congress - Pharmacon China
Mar 2017
The Best of AACC Middle East
Mar 2017
Drug Discovery World Asia
Mar 2017
Classifying Medical Devices - US and EU
Mar 2017
The International Conference on Minimally Invasive Medicine (MIM)
Mar 2017
Pre-Filled Syringes
Mar 2017
PTI - Clinical Research Project Management
Mar 2017
The Conference on Laboratory Medicine and Clinical Research (CLMCR)
Mar 2017
Quality Audits for the Medical Device Industry
Mar 2017
Powers of Attorney: Medical Records Release Concerns
Feb 2017
Trial Master File (TMF): FDA Expectations from Sponsors and Sites
Feb 2017
Annual Biosimilars Summit
Feb 2017
Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigations
Feb 2017
Microsoft Excel Series - Part 3: Beyond IF and Excel Macros
Feb 2017
International Conference on Healthcare, Nursing and Disease Management (HNDM)
Feb 2017
Clinical Trial Monitoring: A Sponsor Responsibility
Feb 2017
Laboratory Inspection Readiness - Implementing GMPS for the Pharmaceutical Laboratory
Feb 2017
Essentials of Complaint Handling and Medical Device Reporting
Feb 2017
Latin America Regulatory Compliance: Current Challenges in Argentina, Brazil and Mexico
Feb 2017
Biosimilar Drug Development World Europe
Feb 2017
Best Practices for Project Management of Clinical Trials
Feb 2017
The Sunshine Act: Reporting for Clinical Trials
Jan 2017
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Jan 2017
GMP for Quality Control and Contract Laboratories
Jan 2017
How to Write HIPAA Policies and Procedures
Jan 2017
Recalls, Removals, and Market Corrections in Compliance with FDA and ISO Requirements
Jan 2017
Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
Jan 2017
Leadership Skills for Scientists Workshop
Jan 2017
Navigating the New European Clinical Trial Regulation (EUCT Regulation 536-2014)
Jan 2017
Transfer of Analytical Methods and Procedures: FDA Requirements and Strategies and Tools for Implementation
Dec 2016
CDRH/Payer Summit for Medical Device Executives
Dec 2016
International Conference on Medicine Management of Hospitalized patient and Healthcare Management (ICMMHPHM)
Dec 2016
Statistical Methods for Design Verification, Process Validation, and Process Control
Dec 2016
Best Practices for FDA Inspection
Dec 2016
Clinical Trial Regulation Conference
Dec 2016
Validation and Part 11 Compliance of Computer Systems and Data
Dec 2016
World Summit on Nanotechnology and Nanomedicine Research
Nov 2016
International Conference on Chest
Nov 2016
Medical Devices - ISO 13485 - Do you really know what you need to?
Nov 2016
Innate Immunity: The line of defence
Nov 2016
Determining Sample Size: How to Ensure You Get the Correct
Nov 2016
Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process
Nov 2016
Design of Experiments for Process/Product Optimization
Nov 2016
Sanitizers for the Food Industry
Nov 2016
In Vitro Diagnostics: Oncology and Infectious Diseases Conference
Nov 2016
Overcoming Data Integrity challenges in Life Sciences
Nov 2016
Good Laboratory Practice Regulations - Introduction and Strategies for Implementation
Nov 2016
Good Laboratory Practices (GLPs) - Comparing and Contrasting with Good Manufacturing Practices (GMPs)
Nov 2016
Laboratory Instrument Calibration: Current FDA Regulatory Requirements and Best Practices
Oct 2016
Laboratory Investigation Out-of-Specification Results
Oct 2016
Exporting Marketing Channel Audits, Importing Marketing Channel Audits, and Logistics Channel Incoterms Standards
Oct 2016
Fundamental Laboratory Record Keeping and Compliance Issue
Oct 2016
Statistical Methods for Design Verification, Process Validation, and Process Control
Oct 2016
Developing Documents and Records to meet the Requirement of ISO 17025
Oct 2016
FDA Inspection: Do`s and Don`ts
Oct 2016
Why is FDA at my facility, and what do I do during an inspection?
Oct 2016
International Forum Healthcare Management (HCM)
Oct 2016
Auditing Clinical Trials for Good Clinical Practice (GCP) Compliance
Oct 2016
Clinical Trial Audits in Practice
Oct 2016
Design and Execution of Stability Studies for Biologics
Oct 2016
MATERIALS` (Ottawa, CANADA:)
Oct 2016
Risk Analysis and Design of Experiments (DOE) in Process Validation and Development
Oct 2016
Medical Devices: US Law, Regulation and Practice
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
Data Integrity: FDA/EU Requirements and Implementation
Oct 2016
Calibration in the Laboratory
Oct 2016
3 Day Masterclass - Clinical Trials
Oct 2016
Artificial Intelligence in Health & Life Sciences Conference
Oct 2016
Production and Process Control: Building a Robust System for Medical Device Companies
Oct 2016
HIPAA Training for the Compliance Officer
Oct 2016
Asia-Pac Trial Master File Summit
Oct 2016
Clinical Trials Supply Chain Forum
Sep 2016
GCP: The IND, How to Gain Approval for Clinical Trials in the USA
Sep 2016
Big Data in Biology and Health
Sep 2016
New Perspectives In Hepatitis C Virus Infection - The Roadmap For Cure
Sep 2016
Ensure Your Healthcare Compliance Program Reaches Optimal Potential and Protect your Organization
Sep 2016
Sub-visible Particulates in Biological products
Sep 2016
Clinical Trial Management Essentials
Sep 2016
Annual Pharmacovigilance Asia
Sep 2016
Investigator Site Files Summit
Sep 2016
Legal, Regulatory and Policy Issues Related to Computer System Validation as the FDA Regulates Tobacco Products
Sep 2016
Implementing ISO 13485:
Sep 2016
Modern Drug discovery and Development Summit
Sep 2016
Defining and Managing Protocol Deviation/Violation/Exception
Sep 2016
The European Microscopy Congress (EMC)
Sep 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
Common Compliance Issues in a Quality Control Laboratory - Data Integrity, Out of Specifications (OOS), Corrective and Preventive Actions (CAPA)
Aug 2016
Meeting the Toughest Laboratory Accreditation Requirements (Part-2)
Aug 2016
Global Medical Device Regulation
Aug 2016
Virus and Pathogen Clearance and Safety in Biologics
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
Lyophilization: What you Need to Know, Validation and Regulatory Approaches
Aug 2016
The CMS Final Infection Control Worksheet for Hospitals
Aug 2016
How to do a Risk Analysis
Aug 2016
Laboratory Safety - Covering Issues such as Compressed Gases, Cryogenic Materials and Glassware, etc.
Aug 2016
What Sample Size Do I Need
Aug 2016
Organic Acids Workshop - San Jose
Aug 2016
How to Prepare for Increased HIPAA Enforcement
Aug 2016
New CMS CoP Regulations for Managing Grievances and Complaints: What Hospitals Should Know about the CMS and Joint Commission and DNV Standards
Aug 2016
International Conference and Exhibition on Cytology & Histology
Aug 2016
Dissolution Testing
Jul 2016
Writing Effective SOPs for the GMP Laboratory
Jul 2016
Creating an Effective Lab Safety Program
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
Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
Jul 2016
Laboratory Management with ISO/IEC 17025:2-Part Series
Jul 2016
Understanding and Implementing an Effective Laboratory Quality Management System to comply with ISO/IEC 17025
Jul 2016
Developing Documents and Records to meet ISO 17025 Requirements
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
BioLogistics Summit
Jun 2016
National Neurotrauma Symposium
Jun 2016
Balkan & National Congress of Nuclear Medicine, BCNM
Jun 2016
Clinical Quality & Compliance Masterclass
Jun 2016
Best Practices for Safety Reporting in Clinical Trials for Drugs, Biologics and Medical Devices
Jun 2016
Mouse Models: Genetics Breeding and Experimental Design
Jun 2016
Verification vs. Validation - Product Process Software and QMS
Jun 2016
Clinical Trial Regulatory Guideline Requirements
Jun 2016
Electronic Data Integrity in a GxP Environment: Managing the Data Lifecycle for Compliance
Jun 2016
Analytical Method Validation under Good Laboratory Practices (GLPs)
Jun 2016
Transfer of Analytical Procedures According to the New USP Chapter [1224]
Jun 2016
Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps)
Jun 2016
International Biopharmaceutical R&D Innovation New Asia Summit
May 2016
Adverse Event Reporting: Site and Sponsor Reporting Requirements for Investigational Products
May 2016
Internal Auditing for the Medical Device Industry
May 2016
Lifecycle Approach to Analytical Methods: Incorporating QbD Principles into Method Development, Validation and Transfe
May 2016
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)
May 2016
Risk Analysis and Design of Experiments (DOE) in Process Validation and Development
May 2016
CHI`s Patient Recruitment & Site Selection
May 2016
Analytical Instrument Qualification and Validation: Understanding to Prepare for FDA Audits to become Part 11 Compliant
May 2016
Italian ePharma Day
May 2016
Validation of a HPLC/UPLC Methodology
May 2016
Nordic ePharma Day
Apr 2016
Design, Analysis and Simulation of Adaptive Clinical Trials Using ADDPLAN
Apr 2016
The Regulatory Framework in Europe
Apr 2016
Data Quality and Technology in Clinical Trials
Apr 2016
The China （Beijing）Medical Equipment Expo
Apr 2016
LABOTEC
Apr 2016
Evaluating the Effectiveness of a Corporate Compliance Program
Mar 2016
Mathematics of Terminal Sterilization - Probability of Survival Approach -vs- Overkill Approach
Mar 2016
Pharma Trials World Asia
Mar 2016
Laboratory Conference
Mar 2016
Antimicrobial effectiveness test USP [51] : Overview and New Content Proposals
Mar 2016
Clinical Innovations Congress Europe
Mar 2016
21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA
Feb 2016
Project management tools to improve productivity and compliance in Analytical laboratories
Feb 2016
Annual Oncology Clinical Trials
Feb 2016
IMDI
Feb 2016
Global Nursing Management Conference
Feb 2016
Modern Approaches to Process Validation: Requirements for Process Design, Design of Facilities and the Qualification of Equipment and Utilities
Feb 2016
Investigational Device Accountability
Jan 2016
Navigating Ethics and Law for Mental Health Professionals: Ethical practice; Risk management, and; Professional codes of ethics
Jan 2016
Cleanroom Monitoring & Maintaining a Quality Environment : Overcoming USP [797] Common Non-Compliance Issues
Jan 2016
Compliant Clinical Research Conduct: What Every Clinical Research Professional Needs to Know
Jan 2016
Good Laboratory Practice Compliance Monitoring Summit
Jan 2016
Avoiding 12 Most Common Statistical Errors in Clinical Research
Jan 2016
FDA`s New Enforcement of 21 CFR Part 11
Jan 2016
From the ER to the OR - IQCP Compliance for CAP Accredited Hospitals
Jan 2016
Accreditation to ISO/IEC 17025:2005- Getting There is Only Half the Fun!
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
Objectionable Microorganisms: Considering the Risk
Dec 2015
French ePharma Day
Nov 2015
Biosimilars Conference
Nov 2015
CNS Clinical Trial Forum
Nov 2015
Development regulatory affairs for Oncology Medicinal Products
Oct 2015
World Open Innovation Forum
Oct 2015
TM`s world drug discovery online conference
Oct 2015
UK ePharma Day
Oct 2015
DIA EMEA
Oct 2015
The Vaccine Summit
Oct 2015
A look at 510(k) changes
Oct 2015
How to manage a successful health authority interaction
Oct 2015
Humanitarian Congress Berlin
Oct 2015
GMP Validation Workshop | Learn to create your own workshop and private sessions
Oct 2015
Personalized Medicine and Its Impact in the Clinic
Oct 2015
Big Data in Clinical Development
Oct 2015
Risk Management in Clinical Trials
Oct 2015
Establishing an FDA-Compliant UDI System
Oct 2015
The Pregnancy Summit
Oct 2015
Orphan Medicinal Product Designation in the EU
Sep 2015
Calibration and Qualification in Analytical Laboratories
Sep 2015
Budgeting for Clinical Trials: Understanding Costs of a Study and Which Costs Sponsors are Responsible to Cover
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
Annual Open Innovation for the Life Science Sector
Sep 2015
Medical Device Regulation in Asia/Pacific Markets
Sep 2015
Auditing QC and Contract Laboratories for GMP Compliance
Sep 2015
Medical Grade Polymers
Sep 2015
FDA`s enforcement of 21 CFR part 11 compliance
Sep 2015
Basic Requirements for Developing IQ and OQ Protocols
Sep 2015
Computer System Validation - Reduce Costs and Avoid 483s: 2-day In-person Seminar
Sep 2015
The Tissue Engineering Congress
Sep 2015
Mobile in Clinical Trials
Sep 2015
The A to Z`s of Microbial Control, Monitoring, Validation and Troubleshooting of Pharmaceutical Water Systems
Sep 2015
Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process
Sep 2015
ISO/IEC 17025:2005 and Laboratory Accreditation
Aug 2015
Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors
Aug 2015
Getting to Know FDA Audit Practices and the 10 Most Common Cited GMP Deficiencies
Aug 2015
PREPARING FOR IMMINENT FEDERAL HIPAA AUDITS (LEVEL:ADVANCE)
Aug 2015
Preparing for Imminent Federal Hipaa Audits (level:intermediate)
Aug 2015
The Statistics of: Design Verification, Process Validation, and Statistical Process Control
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
European Filing and Registration Procedures
Jul 2015
Research Instruments and Equipment Expo & Conference
Jul 2015
USP Hot Topics: What`s Hot Now and How to Track Coming Changes and Influence USP
Jul 2015
Supply-Chain Finance
Jul 2015
Applied Statistics for QA, QC, Manufacturing, and Design Control at SFO
Jul 2015
International Regulatory Cooperation Among Agencies
Jul 2015
Market Access and Commercial Strategy for Healthcare Industry
Jul 2015
Asian IVD Congress & Exhibition Indonesia
Jul 2015
Clinical Research Training for Senior CRAs
Jul 2015
Uncertainty of Measurement as Required by ISO/IEC Standard 17025:2005 for Lab Accreditation:An Environmental Microbiologist’s Perspective
Jul 2015
Beating Malaria
Jul 2015
DIA-TOPRA Workshop on Adaptive Pathways
Jun 2015
Development Regulatory Affairs for Oncology Medicinal Products
Jun 2015
The European Clinical Trial Directive…Plus…European Filings and Registration Procedures
Jun 2015
Biopharmaceutical Raw Materials & Viral Safety for Biologicals
Jun 2015
Premarket Approval (PMA) agreement with FDA for the Medical Device Companies
Jun 2015
Canadian Laboratory Medicine Congress (CLMC)
Jun 2015
South East Asia Regulatory Compliance for Life Science Products, Live Webinar
Jun 2015
Writing Evaluation Reports-How to Write Evaluation Report
Jun 2015
Annual Next Generation Sequencing Data Congress
Jun 2015
U.S. FDA`s New Strategic Priorities 2014 - 1018 ()
Jun 2015
Orphan Drugs Access & Economics Masterclass
Jun 2015
Patient Centric Clinical Trials Europe
Jun 2015
Conducting Observational Studies in US, Canada and Europe
Jun 2015
Quality Assurance for Microbiological Laboratories
Jun 2015
Monitoring Plans: 10 Rules of Effective Writing of Monitoring Plans
May 2015
The FDA Inspection: Preparation, Management, and Follow-Up
May 2015
Developing and Using the Product Risk Management File/Report
May 2015
Crash Course in EU Medical Device Law for Pharma Professionals
May 2015
Practical Application of HIPAA Risk Analysis
May 2015
The A to Z`s of Writing and Enforcing Effective SOPs (Standard Operating Procedures)
May 2015
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU
May 2015
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions
May 2015
MEDTEC France
May 2015
Atlantic Vaccines and Immunotherapeutics Summit
May 2015
Clinical Trial Transparency
Apr 2015
COHORTS, BIG DATA and PERSONALIZED MEDICINE
Apr 2015
International Conference on Advances in Medical Science (ICAMS).
Apr 2015
South East Asia Regulatory Compliance for Life Science Products - Hong Kong, Taiwan, Thailand, Singapore, Malaysia and Vietnam
Apr 2015
Bioinformatics & Drug Discovery Technology
Apr 2015
Is it Method Verification or Validation, or Just Semantics?
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
Issues with Risk Assessments for Cross Contamination of OSD Facilities
Apr 2015
The Need and Role of Standard Operating Procedures in the Pharmaceutical and Medical Device Industries
Apr 2015
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Apr 2015
ICNBS Egypt
Mar 2015
MSL Society Asia Pacific Conference
Mar 2015
Designing Effective and Efficient Extractables or Leachables Studies for Biologics
Mar 2015
Biological Facility Design for Compliance
Mar 2015
BioPharma Manufacturing World Asia
Mar 2015
Complaint-Handling, MDR and Recall Management
Mar 2015
Using Statistical Methods for ICH Guidelines
Mar 2015
Collaboration in Health and Medical Research
Mar 2015
Managing Advanced Research & Development - 2-day In-person Seminar
Mar 2015
Better Alternatives to Sampling Plans
Mar 2015
NGS Milan: Towards Single Cell analysis
Mar 2015
Clinical Drug Development and Approval Process
Mar 2015
Institutional Review Boards (IRBs): The Changing Landscape and the Effect on the Conduct of Clinical Research
Mar 2015
Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Pharmaceutical Water Systems
Mar 2015
Catalyses in Drug Discovery Summit
Feb 2015
Regulatory Filing Strategies Summit
Feb 2015
Complaint Handling and Management: From Receipt to Trending
Feb 2015
How to design and to interpret a clinical trial in the targeted therapies Era
Feb 2015
Key GMP Systems in Pharmaceutical and Biotech Labs
Feb 2015
Health Technology Management Seminar
Feb 2015
Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials
Feb 2015
Clinical Trial Liability Lawsuits
Feb 2015
Blinding of Investigational Materials
Feb 2015
Pre-Filled Syringes
Jan 2015
ADME PK/TK and Drug Metabolism in Drug Discovery and Development
Jan 2015
Personal Medicine and the Future of Health Care
Jan 2015
Benchmark for Cleaning Validation
Jan 2015
Deviations: What are they? Do you need to report?
Jan 2015
Risk-Based Monitoring and the Quality Risk Management of Clinical Trials
Jan 2015
New Requirements for Sponsors and Laboratories for Analyzing Clinical Trial Samples to Meet GCP/GCLP Internationally
Jan 2015
EU Clinical Trial Regulation: New Requirements
Jan 2015
QUANTITATIVE EVALUATION AND MANAGEMENT of Cross Contamination Risks in Multi-Product Facilities
Jan 2015
FDA Decisions For IDE Clinical Investigations
Dec 2014
Cosmetics and the Science of Beautiful Skin
Dec 2014
Therapeutic Antibodies
Dec 2014
Clinical Trial Recruitment Methods and Metrics
Dec 2014
Clinical Research Training for Junior CRAs
Nov 2014
Clinical Project Management
Nov 2014
BIT`s Annual International Conference of Medichem (ICM)
Nov 2014
NGS Nordic - Next Generation Sequencing Symposium
Nov 2014
The Evidence-Based Reimbursement Summit
Nov 2014
What are Serious Adverse Events & How do I Handle SAEs?
Nov 2014
BIT’s Annual World Congress of Endobolism
Nov 2014
European Legislation for Clinical Research – Implementation in Belgium
Nov 2014
NGS Sheffield: from Research to the Clinic
Nov 2014
Health IT & Investment Congress and Exhibition
Nov 2014
XY Congress
Nov 2014
Clinical Trial Inspections: Preparing for a Good Outcome
Nov 2014
Oncology Clinical Development Congress
Oct 2014
Annual Oncology Biomarkers Congress
Oct 2014
Labelling Compliance and UDI Implementation for Medical Devices and IVDs
Oct 2014
Applying ISO14971:2012 and IEC62304 - A Guide to Practical Risk Management
Oct 2014
Legacy System Replacement in an FDA-Regulated Environment
Oct 2014
International Forum Complex support of laboratories (LAB CompLEX)
Oct 2014
Risk Management in Clinical Research
Oct 2014
Drug Discovery Week Europe
Oct 2014
Implementing the Best Practices for FDA Inspection Preparation and Management
Oct 2014
CIO Life Sciences Summit
Oct 2014
Clinical Research for Clinical Trial Assistants
Oct 2014
Circulating Biomarkers
Oct 2014
CUKUROVA MEDICINE
Sep 2014
General Introduction to Clinical Research
Sep 2014
China Vaccine Focus
Sep 2014
Indian Lab Automation (ILA)
Sep 2014
Biomarker Utilisation & Commercialisation
Sep 2014
Global Clinical Trials
Sep 2014
International Conference on Medical and Bioengineering (ICMBE)
Sep 2014
Pursuance of FDA draft guidance on analytical method validation for Drugs and Biologics
Sep 2014
Global Medical Device Regulation: US, EU and Canada at Chicago IL
Sep 2014
Regulatory Affairs & Compliance Consultant David R. Dills Explores ` Advertising and Promotional Requirements for Drugs and Medical Devices` at San Diego
Sep 2014
FDA`s and the U.S. Customs Border Patrol`s Import and Export Control Program
Aug 2014
MEDITECH -International Health Fair
Aug 2014
Statistical Considerations for ICH Guidelines
Aug 2014
International Seminar Establishing the swiftest pathway for registration of Biosimilars in USA
Aug 2014
Auditing, Qualifying and Controlling, Suppliers and Contractors for Pharmaceuticals and Medical Devices (Purchasing Controls)
Jul 2014
Understanding and Implementing the Medical Device Directive
Jul 2014
NGS Workshop Sheffield
Jul 2014
Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data
Jul 2014
Integrating Risk Management into the CAPA System
Jul 2014
CardioVascular Clinical Trialists (CVCT) Asia Forum
Jul 2014
FDA Guidance Design Considerations for Pivotal Clinical Investigations for Medical Devices
Jul 2014
Annual PCT (Partnerships in Clinical Trials) MENA and Turkey
Jun 2014
Best Practices With Submissions Under Medical Device User Fee Act (MDUFA)
Jun 2014
Practical Strategies for Developing Preclinical and Phase I Oral Drug Formulations
Jun 2014
Best Practices for Documenting a Computer System Validation Process
Jun 2014
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
Jun 2014
Global Biosimilars Forum
Jun 2014
Partnerships in Medical Device Trials Conference
Jun 2014
US-China Pharma
May 2014
Sample Prep
May 2014
MediCare
May 2014
GCP and Quality in Clinical Trials
May 2014
Filing Variations
May 2014
Annual European Clinical Data Forum
May 2014
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
May 2014
REHATECH
Apr 2014
GMP Compliance Audit: How Best to Prepare for It
Apr 2014
Companion Diagnostics: From Biomarker Identification to Market Entry
Apr 2014
Moffitt Pathology Symposium: Practicing Pathology in a Changing World
Apr 2014
CMC Analytical, Comparability and Stability Studies
Apr 2014
Annual Clinical Trial Performance Metrics
Apr 2014
Clinical Evaluations & Investigations for Medical Devices
Apr 2014
Risk-Based Approaches to Clinical Trials
Apr 2014
Using Statistical Methods for ICH Guidelines
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
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
Congress of the European Association of Hospitals
Mar 2014
Distribution of Medicines - The New EU Good Distribution Practice Guide...Are You Prepared?
Mar 2014
Disruptive Innovation in Clinical Trials
Mar 2014
Cell Culture Asia
Mar 2014
Implementing Risk Management Principles and Activities within a Quality Management System
Feb 2014
Annual Temperature Maintenance of Pharmaceuticals in Distribution
Feb 2014
BIOLOGICS R&D LEADERS FORUM
Feb 2014
Partnering with Central Labs, Biomarker and Speciality Labs
Feb 2014
Experiences and challenges of setting up biobanks and biobanking networks
Feb 2014
Global Cardiovascular Translational Medicine Conference
Feb 2014
CHI`s Implementing and Managing Strategic Alliances (at SCOPE)
Feb 2014
Good Documentation Practices for Clinical Trials
Feb 2014
Annual Biomanufacturing Summit
Jan 2014
Global Clinical Outsourcing Forum
Jan 2014
Late Phase Drug Development Europe
Dec 2013
Sample Prep East
Dec 2013
Software Validation for the New FDA Inspections - Electronic Records and Electronic Signatures: From 21 CFR Part 11 to HIPAA
Dec 2013
Getting your ADCs to the clinic: Considerations for early stage development
Dec 2013
Conference On Instrumentations & Biotechnologies (CIB)
Nov 2013
Novel Drug Delivery System (NDDS) and Clinical Trial Management China
Nov 2013
API Scale-Up Summit
Nov 2013
Annual Partnerships in Clinical Trials Congress (PCT)
Nov 2013
Clinical Outsourcing for Medical Devices
Nov 2013
Remediating Pharmaceutical Water System Biofilm - What to Do After It Gets Ahead of You
Nov 2013
International summit on GLP, GCP, & Clinical Research
Nov 2013
FDA vs. EU Inspections - How to Prepare and What are the Differences
Nov 2013
Robust Corrective And Preventive Action (CAPA)
Nov 2013
Validations and Resolving Problems Related to Them
Nov 2013
Clinical Trial Supply (CTS)
Nov 2013
Medic East Africa
Nov 2013
510(k) for IVDs
Nov 2013
Unique Device Identification (UDI) Final Rules Overview
Nov 2013
MD&M Minneapolis Expo & Conference
Oct 2013
CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment
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
Falsifying Data in clinical trials. What to report?
Oct 2013
Verification of Compendial Methods According to the Revised USP Chapter <1226>
Oct 2013
Disposable Solutions for Biomanufacturing Summit USA
Oct 2013
WIHE Pharmacy - Warsaw International Healthcare Exhibition
Oct 2013
WIHE Hospital - Warsaw International Healthcare Exhibition
Oct 2013
European Clinical Trial
Oct 2013
Biennial Pathology and Laboratory Medicine Update
Sep 2013
Vacuum Technology in the Process Industry
Sep 2013
Understanding Disinfectant Qualification Studies – How to Avoid Errors
Sep 2013
Clinical Trial Supply USA
Sep 2013
World Biopharma Week China Focus (WBW)
Sep 2013
Asia Global Fair
Aug 2013
Developing and Updating a ``Compliant`` Lab Compliance Plan (Medicare and Medicaid Focus)
Aug 2013
Singapore International Healthcare Week
Aug 2013
Laboratory Medicine Congress
Jul 2013
Oncology Trials Outsourcing
Jul 2013
Future Biotech India
Jul 2013
Clinical Trial Regulatory & Guideline Requirements
Jul 2013
Maximising Pharma Patents
Jun 2013
Biobanking UK
Jun 2013
Optimal capacity planning and resource allocation for a portfolio of clinical trials
Jun 2013
Good Manufacturing Practice (GMP) Annual Training
Jun 2013
Designing Early Phase Clinical Trials
Jun 2013
Mastering Biofilm Control, Monitoring, Validation and Excursion Investigations of Pharmaceutical Water Systems
Jun 2013
Introduction to Bioequivalence and Therapeutic Equivalence
Jun 2013
Shared facilities and the move to science based risk assessments
Jun 2013
Serious Product Quality Problems – Dealing with the Press and the Public
Jun 2013
Ethio Health Exhibition & Congress
Jun 2013
The US FDA Quality System Regulation (QSR) – What Every Exective and Senior Manager Must Know
May 2013
CIMEX - Congo International Medical Expo
Apr 2013
FDA-Compliant Medical Device Reporting (MDR)
Apr 2013
Bridging the Gap: Co-Development of Targeted Therapeutics and Companion diagnostics in the US and EU
Apr 2013
Interactive Response Technologies for Clinical Trials
Apr 2013
China: Compliance Processes for Life Science Products: Company Establishment, Clinical Trials, Registrations - Webinar By GlobalCompliancePanel
Apr 2013
Best Practices for Preparation for, Behavior during, and Response to an FDA Inspection
Apr 2013
Best Practices for Conducting OOS Investigations (in Pharmaceutical Laboratories)
Apr 2013
How to Withstand an FDA Audit of your Facility
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
3-hr Virtual Seminar: Annual ICH GCP Refresher Course
Apr 2013
Designing a Clinical Protocol for Vaccine Clinical Trial
Apr 2013
Life Sciences Market Research
Mar 2013
Bioanalytical Methods Validation
Mar 2013
Quality Practices for Research and Development (R&D) CMC Laboratories
Mar 2013
Good Laboratory Practice Regulations - Introduction and Strategies for Implementation
Mar 2013
Writing Clinical Data Queries - Best Practices and Pitfalls
Mar 2013
FDA Medical Device Approval Process (510(k), IDE, PMA)
Mar 2013
Curtailing Microbial Excursions and Investigations in Pharmaceutical Water Systems
Mar 2013
Risk Assessment - Compliance Using Easy To Fill Out Documentation
Mar 2013
You have a Sterility Failure or Bioburden Excursion - Now What?
Mar 2013
Why are we seeing more Independent Data Safety Monitoring (DMC) use in Clinical Research
Mar 2013
American Healthcare and Natural Products Expo
Mar 2013
3C Contamination Control & Cleanroom Products
Feb 2013
Maximizing the Performance & ROI in Clinical trials: A Personalized Approach
Feb 2013
New Dynamics of Biomarker Labs, Central Labs and ECG & Imaging Labs
Feb 2013
Clinical Laboratory Incident Management Plan - GLP and FDA Compliance
Feb 2013
Advanced Cell Culture & Fermentation - Process Development & Manufacture
Feb 2013
The Clinical Trial Study Protocol (Advanced)
Feb 2013
Environmental Monitoring and Contamination Control Plan
Feb 2013
Making All Data Count: FDA Acceptance of non-US Clinical Trials
Feb 2013
Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection?
Feb 2013
Training on Current ICH GCP Guidelines
Feb 2013
GMP Analytical Laboratory Audits - Planning, Preparation, Execution, and Resolution
Feb 2013
Deviation Management System
Jan 2013
Basic Cell Culture & Fermentation - Process Development & Manufacture
Jan 2013
Objectionable Microorganisms in Medicinal Products - Aseptic Environment
Jan 2013
Life Cycle of Orphan Drug Development & Commercialization
Jan 2013
Optimal Clinical Supply Planning for Global Drug Development
Jan 2013
Patient Reported Outcomes (PROs): Overview and Guidance for clinical trials and medical product labeling
Dec 2012
Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan
Dec 2012
International Summit on GMP & GCP: USA, Europe, Japan, Asia Pacific
Dec 2012
International Conference on Obesity and Weight Management
Dec 2012
Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner -Webinar By GlobalCompliancePanel
Dec 2012
Managing Your Medical Device Reporting (MDR)Program for Compliance Success
Nov 2012
Practical strategies to Improve Productivity in the Pharmaceutical Laboratory
Nov 2012
Auditing Analytical Laboratories for FDA Compliance
Nov 2012
Product Hazard Analysis and Risk Management Under ISO 14971 and FDA, ICH Q9
Nov 2012
FDA Guidance Regarding Clinical Trials for Foods, Food Ingredients, and Dietary Supplements
Nov 2012
Hospital Efficiency Asia
Nov 2012
Sponsor/CRO Forum on Clinical Systems and Process Integration
Nov 2012
Process Validation for Medical Devices
Nov 2012
Design Control for Medical Devices
Nov 2012
Contamination-Control and Cleaning and Disinfection
Nov 2012
Point-of-Care Testing – Neue Herausforderungen an analytische Qualitat und klinische Effizienz
Nov 2012
Aspects to Consider for Clean Room Qualification and Operation
Nov 2012
Annual Forum on PHARMA PATENTS
Oct 2012
Computer Systems Used in Clinical Trials
Oct 2012
Ciamed
Oct 2012
Laboratory Water Systems: Necessary Water Specifications and Validation Challenges
Oct 2012
Avoiding 483 Observations and Warning Letters
Oct 2012
21 CFR Part 11: Ins and Outs of Audit Trails
Oct 2012
Quality Oversight Of Clinical Vendors
Oct 2012
Medifest India
Oct 2012
Live webinar on Preclinical studies regulatory requirements and principle of Good Laboratory Practices (GLP)
Oct 2012
System Based Inspections - Laboratory Controls
Oct 2012
Clinical Trials Drug Supply: Imports and Release Procedures for Shipping to Trial Sites
Oct 2012
21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits
Oct 2012
CDISC – Insight, Impact and Implementation
Sep 2012
Understanding the Decentralised and Mutual Recognition Procedures
Sep 2012
Analytical Method Development, Validation and Transfer
Sep 2012
Clinical Trial Billing - Building a Compliant Process that Works!
Sep 2012
Successful 510(k) submission: Contents and Format
Sep 2012
Medipharm Tanznania
Sep 2012
Update on Unique Device Identifier for Device Manufacturers
Sep 2012
FMEA and Risk Management for Medical Devices
Sep 2012
Optimizing Regulatory Communications and Submissions
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
How to Select Best Practices a CRO ?
Sep 2012
Clinical Trials in Asia (CTA)
Sep 2012
Incorporating Six Sigma DMAIC into CAPA
Sep 2012
Investigator Initiated (Sponsored) Trials – ISSs
Sep 2012
Protein Formulation Development Summit
Sep 2012
Stability Studies for Vaccine Products
Sep 2012
Biosimilars
Sep 2012
Allied Health Scientific Conference
Sep 2012
Annual Early Phase Clinical Trials Asia
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
Addressing Impurities in Pharmaceutical Products: Impurities, Degradants, Residual Solvents and Elemental Impurities
Aug 2012
Process Verification and Validation Planning and Execution
Aug 2012
Human Behavior in Cleanrooms and Controlled Environments - Webinar By GlobalCompliancePanel
Aug 2012
Annual Clinical Research in Emerging Countries
Aug 2012
Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel
Aug 2012
RAPS Approved Seminar on Risk Management in Medical Devices Industry at Mumbai
Aug 2012
CE Marking for Medical Devices Including In Vitro Diagnostic Devices - Webinar By GlobalCompliancePanel
Aug 2012
Sterilization as a Benchmark for Cleaning Validation and Control - 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
New QC Based on Risk Management: A Collaboration between CLIA and CLSI
Jul 2012
Complaint Handling and Management: From Receipt to Trending - Webinar By GlobalCompliancePanel
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
Specialized Formulations – Biomolecules
Jul 2012
HPLC Outside the Box: Beating Your Competitors to Market
Jul 2012
HPLC Outside the Box: How to Think Like a Chromatographer
Jul 2012
Business Development Strategies For Clinical Trials Service Providers
Jul 2012
Navigating the Japan Regulatory and Clinical Trial Environment; Conducting Clinical Studies in Japan
Jul 2012
Clinical Trial Auditing - Identifying risks and building a more compliant and successful trial
Jul 2012
The U.S. FDA`s Tougher Supplier Controls - Webinar By GlobalCompliancePanel
Jul 2012
Good Pharmacovigilance Practice - Inspection and Audits - Webinar By GlobalCompliancePanel
Jul 2012
Obtaining and Marketing Your 510(k) with Today`s FDA, a 510(k) Workshop
Jun 2012
Clinical Trials Supply & Logistics Summit
Jun 2012
Chromatin: from structure to epigenetics
Jun 2012
SLAS Asia Conference and Exhibition - Society for Laboratory Automation and Screening
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
Understanding and Implementing ISO 17025
Jun 2012
Prepare for Tougher cGMP Compliance Audits - Webinar By GlobalCompliancePanel
Jun 2012
Understanding Costs of a Study for Clinical Trials - Webinar By ComplianceOnline
Jun 2012
REMS Update: Risk Evaluation and Mitigation Strategies - Webinar By ComplianceOnline
Jun 2012
Practical Issues with Conducting Multi-National Clinical Trials for Medical Device Approval in the US
Jun 2012
Residual Moisture Testing of Lyophilized Products - Webinar By GlobalCompliancePanel
Jun 2012
Annual Drug Pricing & Reimbursement Forum
Jun 2012
MedicReS World Congress Good Medical Research
Jun 2012
Effective Corrective and Preventive Actions (CAPA): 10 Steps - Webinar By GlobalCompliancePanel
Jun 2012
Implementing Management Responsibility for Medical Devices - Webinar By GlobalCompliancePanel
Jun 2012
The 21 Elements of a 510(k) - Webinar By ComplianceOnline
Jun 2012
Excel Spreadsheet Validation To Eliminate 483s - Webinar by GlobalCompliancePanel
Jun 2012
What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness?
May 2012
Preparing for FDA Inspection and Handling the Consequences
May 2012
MedSib
May 2012
The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems
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
North American Predictive Toxicology Summit
May 2012
Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel
May 2012
Annual What`s New in Anatomic Pathology and Laboratory Medicine
May 2012
FDA Concerns on Alarm Standards and Safety
May 2012
Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
May 2012
Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 2012
International Symposium Interface Biology of Implant (IBI)
May 2012
MEDITECH
May 2012
The International Exhibition on BioPharma, Biotechnology & Equipment (BIOTECH)
May 2012
Integrating Clinical Evaluation and Risk Management
May 2012
Establishing and following Good Clinical Practice (GCP) compliant with the FDA requirements
May 2012
South Korea: Navigating the Clinical Trial and Regulatory Environment - Webinar By GlobalCompliancePanel
May 2012
DHF, DMR, DHR and TF - Regulatory Documents Explained, and Best Practices for Controlling Them
Apr 2012
How to Survive FDA`s `New` Inspection and Enforcement Practices
Apr 2012
IPA Semi-annual Conference on: Cold Chain & Logistics Management
Apr 2012
The Hero of Manufacturing Contamination Control - The Microbiology Lab
Apr 2012
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
IDEM Singapore
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
BioPharma LatAm Convention
Apr 2012
World Vaccine Trials Congress
Apr 2012
Off Label Product Use Discussions in Social Media
Apr 2012
Issue Detection and Escalation in Clinical Trial Settings
Apr 2012
Good Documentation Practices for GXPs
Apr 2012
Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
Apr 2012
Validation and Use of Excel Spreadsheets in Regulated Environments
Apr 2012
Addressing the Challenges of Drug Discovery - Novel Targets, New Chemical Space and Emerging Approaches (F1)
Mar 2012
Medical Device Risk Management Using ISO 14971
Mar 2012
BioPh Japan
Mar 2012
Elegant Quality Assurance Practices for Device Efficacy and Efficiency Requirements
Mar 2012
India Healthcare Congress
Mar 2012
How To Establish An Effective Good Clinical Practice in Drugs and Medical Devices
Mar 2012
Implementing the New USP Chapter <1224> for Analytical Method Transfer
Mar 2012
Business Process Optimization in Pharmacovigilance - Webinar By GlobalCompliancePanel
Mar 2012
Innovations in Healthcare Management and Informatics
Mar 2012
Validation of Bioanalytical Methods and Procedures for FDA Compliance
Mar 2012
Changes in the EU Medical Device Directives; 2010 Modifications and the Recast of the MDD Directives - Webinar By GlobalCompliancePanel
Mar 2012
Advances and Controversies in B-Vitamins and Choline
Mar 2012
Method Validation in Drug Development Process - Common Mistakes and Issues
Mar 2012
Audit/Inspection Preparedness for Clinical Research/Site Coordinators
Mar 2012
Leaping into Lab: Everything about Waived Testing
Feb 2012
Validation of Analytical Procedures for Use in the Pharmaceutical Industry
Feb 2012
Submission Documentation for Sterilization Process Validation - A Comprehensive View of Content for an Approvable CMC Section
Feb 2012
Implement a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
Feb 2012
IASTED International Conference on Biomedical Engineering (BioMed)
Feb 2012
Clinical Trials in Asia
Feb 2012
Quality System Approach and Risk Management for Clinical Trials
Feb 2012
FDA/EU Compliant Training for Laboratory Personnel
Feb 2012
FDA’s Current Thinking for Industry cGMPs for Phase 1 INDs
Feb 2012
Coeur et Diabete (7e edition)
Feb 2012
Investigacion Clinica en Mercados Emergentes: America Latina
Feb 2012
Does your pharmaceutical lab have GMP and non-GMP functions?
Feb 2012
Annual Best Practice Phase IV studies
Feb 2012
Live Web Seminar Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA By compliance2go
Feb 2012
Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical, Biotech, and Medical Device Operations
Feb 2012
How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Feb 2012
Annual Clinical Trials on Oncology
Jan 2012
Preparing for FDA GCP Inspections – Essentials for Sponsor Companies
Jan 2012
Analytical Procedures and Procedures Transfer
Jan 2012
Introduction to the Electronic Common Technical Document
Jan 2012
Quality by Design (QbD) for Development and Validation of Analytical Methods
Jan 2012
Live Web Seminar Design Controls: What to know when it comes to FDA regulated industry? By compliance2go
Jan 2012
New Dietary Ingredients in the Regulatory Scheme
Jan 2012
Troubleshooting Microbial Excursions in Pharmaceutical and Biotech Operations
Jan 2012
DRUG / DEVICE & DEVICE / DRUG COMBINATIONS IN THE EU
Jan 2012
An Introduction to the FDA New Drug Approval Process
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
FDA Compliant Handling of Out of Trend Results in Pharmaceutical Quality Control
Dec 2011
Proven Root Cause Investigation Techniques for Pharmaceutical Water Systems
Dec 2011
GMP Annual Training
Dec 2011
World Influenza Congress Europe
Dec 2011
Conducting Paediatric Clinical Trials
Dec 2011
Introduction to Toxicology for the Non-specialist
Dec 2011
Site feasibility and study start up
Dec 2011
Budget Management for Clinical Trials
Dec 2011
ICSE India
Dec 2011
Analysing Biological Assays
Dec 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
BIT`s World Congress of Small RNAs (WCSR2011)
Nov 2011
Heart, Vessels & Diabetes - The European Conference (2n edition)
Nov 2011
ESSENTIAL GUIDE TO PUBLICATIONS PLANNING - Two Day Course
Nov 2011
Treatment Planning Non-Surgical Periodontal Therapy Cases - Webinar By mentorhealth
Nov 2011
Key Aspects of the Trial Master File and How to Pass FDA Inspection - Webinar By GlobalCompliancePanel
Nov 2011
Cleanroom & HEPA Filter Testing & Certification: An Owners Guide - Webinar by GlobalCompliancePanel
Nov 2011
Equipment Validation, Tracking, Calibration, and Preventive Maintenance - Webinar By GlobalCompliancePanel
Oct 2011
Does your Equipment Program Meet Current Regulatory Expectations - Webinar By GlobalCompliancePanel
Oct 2011
Pharmaceutical & Biopharmaceutical Stability
Oct 2011
Annual Drug Discovery Partnership: Filling the Pipeline
Oct 2011
Live webinar on The FDA Inspection: Preparation, Performance, and Follow-up by compliance2go
Oct 2011
REGULATORY REQUIREMENTS FOR CLINICAL TRIALS - Including an Update on the Proposed Changes to the Clinical Trial Directive Requirements
Oct 2011
analytica Anacon India
Oct 2011
Cell-Based Assays
Oct 2011
Logipharma Boston
Oct 2011
80024480: REWards -- Research Ethics Workshops About Responsibilities and Duties of Scientists (formerly CORE)
Oct 2011
Hybrid Quality Systems For Pharmaceuticals - Combining ICH Q7A & Part 210-211 - Webinar By GlobalCompliancePanel
Sep 2011
Analitica Latin America
Sep 2011
Good Laboratory Practice Regulations: Introduction and Strategies for Implementation
Sep 2011
Understanding Risk Management in Medical Devices
Sep 2011
Animal Models and Their Value in Predicting Drug Efficacy and Toxicity
Sep 2011
EUROanalysis16 - European Conference on Analytical Chemistry
Sep 2011
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go
Sep 2011
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems-By Howard T. Cooper
Sep 2011
RFID in Health Care
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems
Sep 2011
How to design A CAPA System that meets Compliance Requirements
Sep 2011
Ensuring Integrity and Security of Laboratory Data
Sep 2011
Vaccines Asia
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
Preparing for an FDA Pre-Approval Inspection - Webinar By ComplianceOnline
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
Clinical Project Management - Webinar By ComplianceOnline
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
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
80024475: REWards -- Research Ethics Workshops About Responsibilities and Duties of Scientists (formerly CORE) ()
Jul 2011
Translating from Preclinical to Clinical Development
Jun 2011
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
Jun 2011
Ubquitin-Like Molecules in Disease
Jun 2011
Designing an effective cleaning validation in today`s regulatory environment
Jun 2011
Develop and Execute the Company Software V&V Program - Webinar By GlobalCompliancePanel
Jun 2011
Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel
Jun 2011
`The Right Stuff` – Implementing Quality Control Tools in Quality Systems Operations
May 2011
Pharmaceutical and Medical Device Validation Guidance`s - Similarities and Differences - Webinar By GlobalCompliancePanel
May 2011
Sterilization Options for Challenging Products
May 2011
Clinical Trial Technologies and Data Integration Conference
May 2011
Annual Clinical Operations Summit
May 2011
The GCP/ICH Obligations of Sponsors, Monitors, and Investigators - barriers and solution - Webinar By GlobalCompliancePanel
May 2011
Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel
May 2011
CLEAN ROOMS - Standards & Technology
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
Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel
May 2011
FDA`s New Enforcement of 21 CFR Part 11 - Webinar By GlobalCompliancePanel
May 2011
Best Practices for the Implementation and Use of Test Management Tools - Webinar By GlobalCompliancePanel
Apr 2011
Gowning Systems Used in Cleanrooms & Controlled Environments - Webinar By GlobalCompliancePanel
Apr 2011
Avoiding `Failure to Investigate` - Observations by Conducting Effective Investigations
Apr 2011
Proficiency Testing: How to Pass with Flying Colors and What to Do If You Don`t
Apr 2011
Designing appropriate product specifications for lyophilized parenteral products
Apr 2011
Preparing for Pre-approval Inspections - Webinar By GlobalCompliancePanel
Apr 2011
Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel
Apr 2011
The 510(k) Process and Risk Management
Apr 2011
Edition CLINICAL TRIALS IN CANADA
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
Saudi Lab
Apr 2011
REFORMING LABORATORY SERVICES
Apr 2011
Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel
Apr 2011
analytica Vietnam
Apr 2011
FDA`s Revised 510(k) Premarket Notification Process
Apr 2011
ComplianceOnline Webinar - Why and How - Verification of Compendial Methods - USP [1226]
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
Controlled Substances and the Hospital Pharmacy - Webinar By GlobalCompliancePanel
Apr 2011
LAB-TECH
Apr 2011
Understanding the Calibration Curve - Webinar By GlobalCompliancePanel
Mar 2011
European Regulatory Affairs School
Mar 2011
A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - Webinar By GCPanel
Mar 2011
Making Correct Employee- Contractor Classifications
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
2-day In-person Seminar - Electronic Records: Effective Approaches that Reduce Costs
Mar 2011
Meet FDA Expectations for a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
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
Clinical Supply Chain Optimization
Mar 2011
Off-Label Promotion of Drugs - Regulatory Documents Explained - Webinar By GlobalCompliancePanel
Mar 2011
How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant?
Mar 2011
BIO-SAFETY AND BIO-SECURITY
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
The Investigation System (Discovery, Planning, Root Cause Analysis, CAPA) - Webinar By GlobalCompliancePanel
Mar 2011
How to reduce EO residuals in medical devices
Feb 2011
Last changes in Canadian ethics regulations for clinical trial
Feb 2011
Practical Laboratory Statistics - Webinar by GlobalCompliancePanel
Feb 2011
How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters 2010
Feb 2011
Using Foreign Trial Data in Your NDA Approval Process - Webinar By GlobalCompliancePanel
Feb 2011
Annual Clinical Laboratory Educators Conference CLEC
Feb 2011
Eliminate the Confusion –Annex 13 GMP guide
Feb 2011
Responsibilities of a Principal Investigator in Clinical Trials: What you Must Do to Ensure Trial Compliance
Feb 2011
Full Day Virtual Seminar : Annual GLP Refresher Course
Feb 2011
SUSTAINABILITY INPHARMA/LIFE SCIENCES
Feb 2011
CLEAN ROOMS ~Standards &Technology
Feb 2011
LabAutomation
Feb 2011
Webinar on Pharmacovigilance Audit - Webinar By GlobalCompliancePanel
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
How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
Jan 2011
Navigating Pediatric Trials from recruitment to successful on-time completion - Webinar By GlobalCompliancePanel
Jan 2011
Partnering for Cures
Dec 2010
Assessing GCP Compliance in Clinical Trial Audits- Risk management and Best practices - ComplianceOnline Clinical Training
Dec 2010
Good Laboratory Practices - Introduction, Requirements and Tools for Implementation
Dec 2010
Laboratory Investigations Relating to Sample Re-Analysis: Covering the basics before being called out - ComplianceOnline Laboratory Webinar
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
Are you a new Clinical Research Coordinator? Tips on how to get started, what to expect
Nov 2010
Pharma-Bio-Med
Nov 2010
Recent Advances in Microbial Control
Nov 2010
SEBIO
Nov 2010
Full Day Virtual Seminar - Design and Validation of Excel Spreadsheets: Step-by-Step
Oct 2010
ComplianceOnline Virtual Seminar - 21 Cfr Part 11: Complete Manual For Compliance Success
Oct 2010
ComplianceOnline Webinar - Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137 ()
Oct 2010
The Tougher U.S. FDA - One Year Later
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
The FDA Tripod - Clinical Trial Regulations, Compliance and GCP in Drug Development
Oct 2010
ComplianceOnline Webinar - GMPs in Biopharmaceutical Development Laboratories
Oct 2010
Best Practices for Managing FDA Investigators and Handling FDA 483 Observations
Sep 2010
Ensuring GCP compliance through quality auditing in clinical trial
Sep 2010
Tagung der Arbeitsgemeinschaft Akkreditierter Laboratorien (AAL)
Sep 2010
Understanding and Preparing for FDA`s New Part 11 Inspection Program
Sep 2010
IC and ESSCA ( European Course on Clinical Cytometry, Euroconference on Clinical Cell Analysis)
Sep 2010
The ICF Process: Tips on Achieving Optimal compliance and Comprehension
Sep 2010
Quality by Design (QbD) and Analytical Methods - Webinar by GlobalCompliancePanel
Sep 2010
Developing Supplier Quality Auditor Training Programs
Sep 2010
Astana Zdorovie - International Kazakhstan Exhibition on Healthcare
Sep 2010
Verification of Pharmacopeia Methods - Webinar by GlobalCompliancePanel
Sep 2010
ComplianceOnline Webinar - Controlling Change to meet GMP Requirements
Sep 2010
Effective & Essential CAPA process to avoid FDA 483 - Webinar by GlobalCompliancePanel
Sep 2010
Good Documentation Practices for GMP Operations - Webinar by GlobalCompliancePanel
Sep 2010
ComplianceOnline Webinar - Streamline Documentation System in Pharmaceutical Laboratory
Aug 2010
Conducting Value Added Audits of Technical Service Providers - Webinar by GlobalCompliancepanel
Aug 2010
Method Transfer of Analytical Methods - Webinar by GlobalCompliancepanel
Aug 2010
System Based Inspections - The Laboratory Control System
Aug 2010

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