Online Events on Medical technology (past events)

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Showing 531 conferences
International Congress on Biomedical Engineering
Oct 2024
International Conference on Advances in Biological Science and Technology (ICABST)
Sep 2024
International Conference on Bioscience & Engineering (BIOSE)
Sep 2024
Modernize Clinical Technology
Aug 2024
International Conference on Photonics, Optics and Laser Technology
Aug 2024
International Forum on Biotechnology and Genetic Engineering (BIOTECHFORUM)
Jul 2024
Global Meet on Public Health and Healthcare Management (GMPHHM)
Jun 2024
CIO/CISO Healthcare Summit
Dec 2023
Global Summit and Expo on Biotechnology and Bioscience (GSEBB)
Oct 2023
Evaluating Biopharma: Continuous Bioprocessing
Oct 2023
Smart(er) Biomanufacturing: Evaluating the Risks and Opportunities
Sep 2023
4the International Precision Medicine Conference
Aug 2023
International Conference on Vaccines: Research and Development
Jul 2023
Sri Lanka Medical Association (SLMA) International Medical Congress
Jul 2023
Purification: New Technologies and Strategies to Support Complex Molecules
Jun 2023
International Conference on Parkinson`s Disease and Movement Disorders
Jun 2023
The International Respati Health Conference (IRHC)
Mar 2023
Global Congress on Healthcare and Technologies
Mar 2023
Evaluating Biopharma - Cell Culture Optimization
Feb 2023
3D Medical Printing Conference & Expo
Feb 2023
International Congress on Biomedical and Bio Instrumentation (ICBBI)
Feb 2023
International Conference on Endocrinology (ICOE)
Jan 2023
Strategy for Cell & Gene Therapies
Jan 2023
Eurasia Gulf Online Startup Forum
Dec 2022
Evaluating Biopharma - Cell Therapy Strategies
Dec 2022
Eternity Life Forum
Nov 2022
iMerit x TechCrunch ML DataOps Summit
Nov 2022
HPAPI Handling & Manufacturing Summit
Sep 2022
International Conference on Healthcare Engineering (ICHE)
Sep 2022
International Conference on Nanomedicine and Drug delivery
Sep 2022
PK/PD in Drug Discovery and Development for the US market MasterClass
Sep 2022
International Summit on Nanomedicine & Nanotechnology
Jul 2022
International Conference on Biomedical Engineering (ICBME)
Jul 2022
International Conference on Pharmaceutics and Novel Drug Delivery Systems
Jun 2022
MENA Pharmacy Congress
Jun 2022
Pre Event Respiratory Drugs
Jun 2022
JAK Inhibitors Drug Development Summit
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
The International Conference on Information and Communication Technologies for Ageing Well and e-Health (ICT4AWE)
Apr 2022
International Conference on Molecular Medicine and Diagnostics
Apr 2022
3D Cell Culture
Feb 2022
The EAAR Conference on New Medical Device Regulations (RMD2022)
Feb 2022
Speaker Programs and Advisory Boards
Jan 2022
International webinar on Anatomy and Physiology
Dec 2021
International Conference on Medical Imaging Science and Technology (MIST)
Dec 2021
Meet on Digital Health
Nov 2021
Aesthetic & Cosmetic Regulatory Events Summit (ACRAS)
Nov 2021
International Virtual Conference on Clinical Trials and Case Reports
Nov 2021
Wnt & B-Catenin Targeted Drug Discovery Summit
Nov 2021
Regulatory and Technology Considerations for the Design of Medical Device Software MasterClass
Nov 2021
Early & Managed Access Programmes
Nov 2021
Healthcare Quality and Safety
Oct 2021
Medical Device Digi Expo
Oct 2021
Combination Products Summit
Oct 2021
Critical Quality Attributes of Recombinant Proteins for Therapeutic Use MasterClass
Sep 2021
Xcelerate at Biotech Week Boston
Sep 2021
How to submit variations in Europe MasterClass
Sep 2021
MedTech & Diagnostics Value & Access USA
Sep 2021
Advanced Precision Medicine MasterClass
Sep 2021
WorldFestival
Aug 2021
International Conference on Advanced Pharmacy and Clinical Research
Aug 2021
National Institute for Health and Care Excellence (NICE), UK: Transformation in Action
Aug 2021
Decoding Digital Health for Life Sciences
Jun 2021
Society of Nuclear Medicine and Molecular Imaging (SNMMI) Annual Meeting
Jun 2021
Nanotechnology and Nanomedicine (iNano)
Jun 2021
Digital innovations in health and care
May 2021
European Health-Tech Innovation Week
May 2021
ProcureCon Pharma
May 2021
Artificial Intelligence Symposium
May 2021
Asia-Pacific Pharma Congress
May 2021
International Conference on Nanomedicine and Nanotechnology
Apr 2021
Personalized and Precision Medicine International Conference (PEMED)
Apr 2021
Global Clinical Quality Conference
Apr 2021
Medical Device R&D Summit
Mar 2021
Sri Lanka Medical & Equipment Virtual Expo
Mar 2021
UAE TeleHealth Conference
Mar 2021
Drug Delivery Devices Symposium
Mar 2021
Medical Writing for Medical Devices
Mar 2021
IEEE International Conference on E-health Networking, Application & Services (Healthcom)
Mar 2021
Ventricular Assist Device (VAD) CME Symposium for Community Partners
Feb 2021
Molecular Med TRI-CON
Feb 2021
MedAffairs for MedTech & Diagnostics
Feb 2021
Spotlight Telemedicine​ - International Summit on Innovation and Technology
Jan 2021
Gastroenterology and Hepatology Congress
Jan 2021
PepTalk: The Protein Science Week
Jan 2021
Clinically Validated Digital Therapeutics Summit
Dec 2020
Product Launch Excellence for Pharma & Biotech
Nov 2020
CAR-T Beyond Oncology Digital Event
Nov 2020
Handelsblatt: Health - The Digital Future
Nov 2020
International Conference on Wound Care, Tissue Repair and Regenerative Medicine
Oct 2020
International Conference On Orthopedics & Advanced Care
Oct 2020
Clinical Innovation and Supply Chain Management
Oct 2020
Global Experts Meet on Biotechnology and Biomedical Engineering
Oct 2020
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering Training
Oct 2020
BODYNETS - EAI International Conference on Body Area Networks
Oct 2020
Med-Tech & Med-Cann World Summit
Oct 2020
DigiHealthSouth - EAI International Conference on Digital Healthcare Technologies for the Global South
Oct 2020
Global Conference on Stem Cell & Regenerative Medicine
Oct 2020
Global Forum for Qualified Person for Pharmacovigilance (QPPV)
Oct 2020
Digitalpathology
Oct 2020
Digital Clinical Biomarkers and World CDx Summit
Oct 2020
EuroSciCon Conference on Biotechnology & Bioengineering
Sep 2020
Virtual Health Care Summit
Sep 2020
WIRED Health:Tech
Sep 2020
International Dentistry and Dental Public Health Conference
Aug 2020
Fierce AI Week
Aug 2020
Euro Biosensors and Bioelectronics Conference
Aug 2020
International Conference on Nursing and Palliative Medicine
Aug 2020
International conference on Nanotechnology and Nanomedicine
Jul 2020
PREDiCT: Imaging Modalities For Oncology Drug Development Summit
Jun 2020
TechXchange: Healthcare & Life Sciences
Jun 2020
Digital Health Online Summit
May 2020
Key Factors to Write an Effective Standard Operating Procedure (SOP) and Work Instructions (WIs)
Feb 2020
Audit Trail Generation and Review
Feb 2020
Confidentiality of Substance Use Disorder Patient Records; Complying with the New Federal Law 42 CFR Part 2
Nov 2019
Adjustable Rate Mortgage (ARM) Rule
Aug 2019
Requirements for IQ, OQ and PQ Quality Protocols
Aug 2019
6-Hour Virtual Seminar on Adaptive Design for Clinical Trials
Jul 2019
Basics of Testing Associated with Sterilization Validation and Routine Processing
Jul 2019
Onboarding: From Entry-Level to Senior Executive
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
Are you responsible for Enterprise Risk Management Compliance: How to conduct a Compliance Gap Analysis for ERM, how to get started and what to expect?
May 2019
FDAs Quality Metrics - Latest Advances
May 2019
Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry
May 2019
The Value of a Human Factors Program
May 2019
Texting and Mobile Devices in Healthcare - HIPAA and CMS Requirements for Security of PHI
May 2019
ISO 62304 How to Create a Medical Software Development File?
May 2019
Quality by Design (QbD) in Pharmaceutical and Medical Device Manufacturing
May 2019
Effective Records Management and Document Control for Medical Devices
May 2019
Quality Control for Microbiological Media and Reagents
May 2019
Quality Risk Management Overview
May 2019
Compliance Measures for Case Managers
May 2019
Fishbone Diagramming
May 2019
Continued Process Verification - A Systematic Approach
Apr 2019
Ensuring your Site is Ready for an FDA Inspection
Apr 2019
IEC 62304 for Medical Device Software
Apr 2019
FDA`s New Import Program for
Apr 2019
Test Method Validation to Verify the Performance of a Medical Device
Apr 2019
Medical Device Laws and Regulations in Asia – Part 1 – China
Apr 2019
Medical Device Laws and Regulations in Asia – 2 Part Web-Series
Apr 2019
Analytical Method Validation and Transfer
Apr 2019
Compliance with the New ICH GCP Revision 2 Addendum
Apr 2019
Current Trends in CyberSecurity Threats to Medical Devices
Mar 2019
EO Sterilization Validation / Revalidation per ISO 11135
Mar 2019
Dealing with OCD in the Office
Mar 2019
FDA`s Quality Metrics - Latest Advances
Mar 2019
What is Human Factors and why is it Important?
Mar 2019
FDA`s Scrutiny of Social Media Promotion
Mar 2019
Additive / 3D Printing Manufacturing and Its Regulatory Issues
Mar 2019
Handling OOS Test Results and Completing Robust Investigations
Mar 2019
Establishing a Medical Device Security Program
Feb 2019
Analytical Method Transfer According to USP General Chapter-1224
Feb 2019
Design Verification, Validation and Testing for Medical Devices
Feb 2019
Understanding FDA Design Verification and Validation Requirements for Medical Devices
Feb 2019
Translating Academic Assays for GLP Use
Jan 2019
ICH GCP Guidelines E6 Revision, R2 Addendum- Changes Impacting Sponsors-CRO-Sites
Jan 2019
Mastering Excel Pivot Tables
Jan 2019
Sample Size Determination for Design Validation Activities
Dec 2018
In a Nutshell: Data Protection & Privacy Legislation in the U.S. & European Union
Dec 2018
Handling Situations Where Regulation E and ACH Don`t Align
Dec 2018
Seasonal Influenza Vaccines- Current Concepts and Future Trends for Effective Immunization
Dec 2018
Medical Devices - ISO 13485
Dec 2018
Best Practice When Assessing Social Communication with High Functioning Autism Spectrum Disorders
Dec 2018
How to use the Environment to Address Arousal and Hyperactivity
Dec 2018
Drafting a Software Verification and Validation Report Package and Protocol - The 11 Must-have Documents
Dec 2018
Excel Formulas and Functions
Nov 2018
Control-Analysis Instrumentation used in PAT Continuous Manufacturing
Nov 2018
Data Integrity in Clinical Trials
Nov 2018
Risk Management Techniques for Medical Devices
Nov 2018
How to Write SOPs which are Compliant for Inspections for a GXP Compliance
Nov 2018
Disaster Recovery and Business Continuity Planning for Computer Systems Regulated by FDA
Nov 2018
Advanced Formulas & Functions in Excel
Nov 2018
Validation Sampling Plans for Process Validation, Design Verification and CAPA Effectiveness Checks
Nov 2018
Simple Compliance Steps for Email and Texting to Save Providers from Serious, Widespread HIPAA Violations
Oct 2018
How People with Depression Think - How to Help
Oct 2018
Sterilization of Pharmaceutical Products and Medical Devices
Oct 2018
Metrology: Statistical Analysis of Measurement Uncertainty
Oct 2018
Pharmaceutical Compressed Air - Quality GMP Requirements
Oct 2018
Employment Agreements, Contractor Agreements & Negotiating Skills
Oct 2018
Secrets to Writing Effective SOPs for Medical Device QMS
Oct 2018
Medical Device Hazard Analysis Following ISO 14971
Oct 2018
HIPAA Breach - Or Not? How to Find Out & What to Do
Sep 2018
Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success
Sep 2018
Understanding Autism Spectrum Disorder (ASD): Preparing Students to Transition to College and Succeed
Sep 2018
Vendor Selection and Management
Sep 2018
Marketing to Medicare or Medicaid Beneficiaries - What You Can and Cannot Do
Aug 2018
Supply Chain Issues (21 CFR Part 820.50 and 820.80) and Warning Letters
Aug 2018
FDA`s Revolutionary Change in Software Regulation
Aug 2018
HIPAA Training for Compliance Officer
Aug 2018
HIPAA Breach Evaluation and Reporting - What Qualifies as a Reportable Breach and how to Report It
Aug 2018
What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections
Aug 2018
CMS Hospital CoP and TJC Telemedicine Standards, Telemedicine Credentialing and Privileging
Jul 2018
Laboratory Investigations for Out of Specification Results
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay that Way
Jul 2018
Hospital System Complications and Conflicts: Mergers, Acquisitions, and the Medical Staff
Jul 2018
Deviation Investigation Best Practices: Ensuring Correct Content and Conclusions
Jul 2018
Patients Suing Under HIPAA
Jul 2018
510(k) Documentation Best Practices for Software or Software Enabled Medical Devices
Jun 2018
Ligature Risks: Ensuring Compliance with the CMS Hospital CoPs and TJC Requirements
Jun 2018
Food Fraud in the Organic Industry
Jun 2018
Overview of Medical Device Regulation in Europe
Jun 2018
Document Control and Change Control Process in GxP/GMP Environment
Jun 2018
The Safety Maturity Curve - Where does your Organization Stand?
Jun 2018
Criteria for IRB Approval - Essential Training for IRB Members and Staff
Jun 2018
Off label Promotion of Drugs and Medical Devices - FDA`s Latest
Jun 2018
Why and How - Verification of Compendial Methods - USP [1226]
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
Health Product Marketing authorization in Brazil - Documentation, Approval Process, Labeling, Advertising and Post Market Vigilance
May 2018
Fundamentals of Risk Management in Clinical Research
May 2018
How to Comply with 21 CFR 11 Requirements for Electronic Medical Records
May 2018
Driving a Quality-Lean Steering Committee
Apr 2018
Failure Modes and Effects Analysis
Apr 2018
Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities
Apr 2018
Differences Between ISO 13485 & ISO 9001 - and How to Choose Which One to Implement
Apr 2018
Medical Device Single Audit Program (MDSAP) Preparation
Apr 2018
European Data Protection Regulation - Implementation
Mar 2018
Key Legal Considerations When Redesigning Your Physician Compensation Plans
Mar 2018
Telemedicine: Coding, Billing and Compliance
Mar 2018
Ambulatory Surgery Centre Updates
Mar 2018
Developing a Physician Compensation Strategy Focused on Quality and Value
Mar 2018
The Patient Experience: The Direct Path to Better Clinical Outcomes
Feb 2018
CPT and HCPCS Updates
Feb 2018
21 CFR Part 11 Compliance - Ensuring Data Integrity and Safety in Clinical Research
Jan 2018
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
Dec 2017
Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices
Dec 2017
Equipment and Facility Qualification
Dec 2017
Analytical Method Validation Under Good Laboratory Practices - GLPs
Dec 2017
Dealing with Performance Issues
Nov 2017
AAMI TIR 45: Agile Meets Software Standards, and we all Win
Nov 2017
FDA`s Latest Regulations for Tobacco Industry Effective 8-2016
Nov 2017
Medical Device Hazard Analysis Following ISO 14971
Nov 2017
The Future of Supply Chain - 7 Megatrends that will Transform the Global Marketplace
Nov 2017
Virtual Seminar on Analytical Method Validation Process
Nov 2017
Compliance Requirements for Compounding Pharmacies Based on USP Chapters 795, 797, and 800
Nov 2017
World Clinical Medicine & Collaboration Forums
Oct 2017
Medical Device Engineering Change Control
Oct 2017
Document Control and Training
Sep 2017
Essentials of Validation -IQ,OQ,PQ
Sep 2017
Investigation of Out-Of-Specification Laboratory Results
Sep 2017
New Relationship between the Data Controller, Data Processor and the Data Subject
Sep 2017
FDA`s Medical Device Clinical Trials Program
Aug 2017
Device Accessories - Understanding and Implementing the Final Guidance Document
Aug 2017
FDA Regulations for Environmental Monitoring (EM) Program
Aug 2017
Building a Validation Program From Top to Bottom
Aug 2017
Applying Human Factors and Usability Engineering Throughout the Medical Device Development Lifecycle
Jul 2017
How To Establish an Effective Chief Compliance Officer`s (CCO) or Chief Risk Officer`s (CRO) Function - Organization and Responsibilities
Jun 2017
Complaints, Servicing and FDA Reporting
Jun 2017
Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations
Jun 2017
Healthcare Medical Software/Applications - Risks, Validation & Interoperability
Jun 2017
FDA`s Expedited Development and Approval Programs: Taking the Mystery out of Expedited Approvals
May 2017
New FDA or EMA and USP Guidelines for Transfer of Analytical Methods
May 2017
Phase I GMPs
May 2017
Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations
May 2017
Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner
May 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
Medical Necessity: Can you define it, Capture it, Document it
Apr 2017
Pharmaceutical and Biologics Facility Design: FDA and Regulatory Aspects
Apr 2017
Inclusion of LGBT Employees in Healthcare: Navigating Policies, Procedures, and Practices
Apr 2017
Telemedicine and being Compliant
Mar 2017
Classifying Medical Devices - US and EU
Mar 2017
Telehealth: Understanding JCAHO Standards and Legal Regulatory Compliance
Mar 2017
21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration
Feb 2017
Powers of Attorney: Medical Records Release Concerns
Feb 2017
Trial Master File (TMF): FDA Expectations from Sponsors and Sites
Feb 2017
CMS Hospital Improvement Act Proposed Changes: Nursing, Medical Records, Infection Control, Antibiotic Stewardship Program, Restraints, QAPI and much more!
Feb 2017
Microsoft Excel Series - Part 3: Beyond IF and Excel Macros
Feb 2017
Electronic Health Records Software License Agreements: Common Terms and Concerns
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
Three-dimensional cell culture: Innovations in tissue scaffolds and biomimetic systems
Feb 2017
Spotlight on Post Market Surveillance
Feb 2017
How to conduct a Human Factors and Usability validation following ISO62366 and the new FDA Guidance
Feb 2017
Requirements for Registration of Medical Device Products in China
Jan 2017
Microsoft Excel Macros-4-Part Series: Your Key to Success In The Modern Business World
Jan 2017
Microsoft Excel Series - Part 1: Shake Hands with Macros
Jan 2017
Ensuring Compliance with ICH GCP E6 (R2) Requirements: Meeting the challenges of RBM
Jan 2017
New Technologies Affecting Healthcare
Jan 2017
Implementation of Risk Evaluation and Mitigation Strategy (REMS) Programs in a Health System
Jan 2017
Implementation of the Generic Drug Labeling Rules
Jan 2017
HIPAA Breach Notification Rule - What you must do to Comply
Jan 2017
National Consumer Assistance Plan
Jan 2017
Fundamentals of the de novo process for medical devices: What you need to know when pursuing a de novo application and approval with the FDA
Jan 2017
Effective Corrective and Preventive Action Program (CAPA): The Role of Corrective Action and Preventative Action in Your Quality Management System
Jan 2017
Reinventing Remote Monitoring to Improve Clinical Trial Quality
Dec 2016
Go Beyond ISO 9001:2015`s Requirements when Dealing with Risk
Dec 2016
Managing the IDE (Investigational Device Exemption) Submission for Compliance Success
Dec 2016
Editing Your Own Work (After you`ve read it 1000 times)
Nov 2016
Innate Immunity: The line of defence
Nov 2016
Sanitizers for the Food Industry
Nov 2016
Risks of Omission
Nov 2016
Vaccine Antigen Delivery: new approaches to vaccine development
Oct 2016
MEDDEV 2.7.1, Revision 4 for Clinical Evaluation and the Latest Guideline: A Guide for Manufacturers and Notified Bodies
Oct 2016
HIPAA Training for the Compliance Officer
Oct 2016
Production and Process Control: Building a Robust System for Medical Device Companies
Oct 2016
2017 Proposed Home Health PPS Rule: Pre-Payment Review and Other Regulatory Developments
Sep 2016
Setting and Measuring Quality Objectives
Sep 2016
Texting and E-mail With Patients Under HIPAA
Sep 2016
Medical Record Standards: What Hospitals Should Know About the CMS Hospital CoPs
Sep 2016
How to prepare for and Host FDA Inspection and Avoid 483`s
Sep 2016
FDA and CFIA-Overview of Proposed Regulations - Let`s Get Updated
Sep 2016
Moving Forward with Stem Cell Therapy
Sep 2016
Reducing Drug and Device Batch Release Times: Improving your BPR/DHR Review and Assessment
Sep 2016
Handling, Storage, Distribution, and Installation of Medical Devices
Sep 2016
FDA Regulation of Digital Health - Current Status and Recent Developments
Aug 2016
Business Continuity or Disaster Recovery Planning
Aug 2016
Lyophilization: What you Need to Know, Validation and Regulatory Approaches
Aug 2016
Changes to the Common Rule (45 CFR 46) : What this means for you
Aug 2016
How to do a Risk Analysis
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
Final Rules for Electronic Health Records Stage 3 Meaningful Use Update
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
FDA`s Low-Risk Device Policy and the Impact on Mobile Medical Device Applications
Jun 2016
Investigating and Reporting Adverse Reactions Related to Human Cells, Tissues, and Cellular and Tissue Based Products (HCT/Ps)
Jun 2016
Complying With Telemedicine Requirements
May 2016
Disposition of Records and Records Retention for Medical Records, Including Electronic Records
May 2016
An Ethical Use of Electronics, EHR, and e-Anything
May 2016
Best Practices for Compliance with FDA 21CFR1040
Apr 2016
Claims Follow Up, Appeals and Self Pay Collections
Apr 2016
The Importance of the Investigator Responsibilities and Legal Commitments in Drug and Device Clinical Research in Achieving a Clean Audit
Apr 2016
Medical Coding, Billing and Documentation
Apr 2016
The New Clinical Trial Regulation
Apr 2016
Medical Identity Theft and Data Breaches
Mar 2016
Ensuring Compliance of Your Bioanalytical Method Validation with the 2013 FDA Draft Guidance
Mar 2016
Antimicrobial effectiveness test USP [51] : Overview and New Content Proposals
Mar 2016
Device Changes and the 510(k)
Mar 2016
Medicare Penalties and Incentives – Update for Medical Practices
Jan 2016
Avoiding 12 Most Common Statistical Errors in Clinical Research
Jan 2016
Developing a Validation Master Plan
Dec 2015
Effective Strategy for Medical Device Recalls
Nov 2015
ObamaCare Takes Aim at Healthcare Fraud and Abuse
Oct 2015
Is your Essential Requirements Checklist (ERC) up to snuff?
Oct 2015
Science of Safe Care: Understanding Patient Centered Care
Oct 2015
Risk-based Supplier Management System: ImpactImpact on Regulatory and Operational Goals for Medical Device Manufacturers
Sep 2015
Managing Mobile Devices in Healthcare — Know How to Protect PHI and Comply with HIPAA
Sep 2015
Designing Medical Devices for Long Life at Lower Costs
Sep 2015
Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors
Aug 2015
Medical Device Recalls
Aug 2015
Understanding ISO 13485-FDA Requirements for Medical Devices
Aug 2015
PREPARING FOR IMMINENT FEDERAL HIPAA AUDITS (LEVEL:ADVANCE)
Aug 2015
Preparing for Imminent Federal Hipaa Audits (level:intermediate)
Aug 2015
How To Conduct Medical Device Risk Analysis Effectively (level: Advance)
Aug 2015
Understanding the Mobile Medical Applications Guidance
Aug 2015
European Filing and Registration Procedures
Jul 2015
Pest Control in Food Processing and Foodservice
Jul 2015
Supply-Chain Finance
Jul 2015
Mastering Medical Decision Making
Jul 2015
International Regulatory Cooperation Among Agencies
Jul 2015
Medical Necessity: Clinical Medical Necessity vs Billing Medical Necessity
Jul 2015
Advances in Robotic Inspection as Applied to Orthopedic Implants
Jul 2015
Development Regulatory Affairs for Oncology Medicinal Products
Jun 2015
Software Verification and Validation in Medical Industry
Jun 2015
Medical Staff Fair Hearings- Lawsuit-Proof Process Tips
Jun 2015
Premarket Approval (PMA) agreement with FDA for the Medical Device Companies
Jun 2015
Normality Tests and Normality Transformations
Jun 2015
Understanding Regulation of Orphan Devices: Humanitarian Device Exemptions (HDEs) and Humanitarian Use Designations (HUDs)
Jun 2015
Supplier Quality Management - Implement it Now or Pay for it Later
Jun 2015
International Online Medical Conference (IOMC)
May 2015
Monitoring Plans: 10 Rules of Effective Writing of Monitoring Plans
May 2015
Regulatory Inspections: The Art of Managing the Investigator
May 2015
Developing and Using the Product Risk Management File/Report
May 2015
Writing Effective Journal Abstracts: A Guide for Medical Writers and Clinical Research Professionals
May 2015
Foreign Bodies in Foods - Effective Techniques for Prevention, Control and Detection
May 2015
MDRs - Bureaucracy or Benefit
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
Newest Developments in Medical Diagnostics & Therapy for All Health Professionals
Mar 2015
Laboratory Developed Tests under FDA`s Thumb
Mar 2015
Telehealth and Regulation of Health Care Services Delivered via Telehealth
Feb 2015
Personal Medicine and the Future of Health Care
Jan 2015
New Requirements for Sponsors and Laboratories for Analyzing Clinical Trial Samples to Meet GCP/GCLP Internationally
Jan 2015
FDA Decisions For IDE Clinical Investigations
Dec 2014
How to Create, Manage and Implement a Coding Compliance Plan
Dec 2014
How to Develop an Effective Compliance Program
Oct 2014
Legacy System Replacement in an FDA-Regulated Environment
Oct 2014
Pursuance of FDA draft guidance on analytical method validation for Drugs and Biologics
Sep 2014
Current Good Manufacturing Practices (cGMP) for Medical Devices and IVDs
Sep 2014
Batch Production Record and Device History Record Review and Quality Assessment
Aug 2014
Auditing, Qualifying and Controlling, Suppliers and Contractors for Pharmaceuticals and Medical Devices (Purchasing Controls)
Jul 2014
HIPAA Compliance Though Policies
Jul 2014
Cleaning, Maintenance and Calibration Programs: Critical Programs but Often Overlooked
Jul 2014
To file or not to file an NDA Application: When GCP Noncompliance Compromises your Pivotal Trial
Jul 2014
FDA Guidance Design Considerations for Pivotal Clinical Investigations for Medical Devices
Jul 2014
Best Practices With Submissions Under Medical Device User Fee Act (MDUFA)
Jun 2014
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
Jun 2014
GMP Compliance Audit: How Best to Prepare for It
Apr 2014
Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
Mar 2014
Clinical Trial Design for Personalised Medicine Webinar
Nov 2013
Robust Corrective And Preventive Action (CAPA)
Nov 2013
510(k) for IVDs
Nov 2013
Unique Device Identification (UDI) Final Rules Overview
Nov 2013
Process Capability Indices in Medical Device Manufacturing
Oct 2013
FDA`s Oversight of Mobile Medical Applications (`apps`) for Use on Smartphones and Similar Mobile Devices
Sep 2013
How to Manage a Medical Device Recall Efficiently and Effectively
Jul 2013
Construct and Manage the Technical File and Design Dossier
Jul 2013
Optimal capacity planning and resource allocation for a portfolio of clinical trials
Jun 2013
The US FDA Quality System Regulation (QSR) – What Every Exective and Senior Manager Must Know
May 2013
e-Submissions & Data Standards for FDA (eCTD, CDISC, HL7)
May 2013
FDA-Compliant Medical Device Reporting (MDR)
Apr 2013
e-Submissions & Data Standards for FDA (eCTD, CDISC, HL7)
Apr 2013
Bridging the Gap: Co-Development of Targeted Therapeutics and Companion diagnostics in the US and EU
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
Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Variable Data
Apr 2013
New EU Pharmacovigilance Directive and Regulations
Apr 2013
Effective, Risk Based Implementation of the Quality Systems
Apr 2013
When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation
Apr 2013
Ten-Step Process for COTS Computer System Validation - Reduce Time and Costs - GlobalCompliancePanel
Apr 2013
FDA QSR Acceptance Activities - Webinar By GlobalCompliancePanel
Apr 2013
Medicare and Medicaid EHR Incentives for Eligible Professionals & Hospitals
Apr 2013
Best Practices in Document Approval, Control, and Distribution
Mar 2013
Transferring a Medical OEM Molding and Assembly Operation to a Manufacturer With Validated Systems and Processes
Mar 2013
Engineering Change Management for Pharmaceutical Capital Projects
Mar 2013
Training on Current ICH GCP Guidelines
Feb 2013
Deviation Management System
Jan 2013
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
Ensuring Integrity and Security of Electronic Records for FDA Compliance
Nov 2012
Good Deviation Practice: what you need to know
Nov 2012
FDA Guidance Regarding Clinical Trials for Foods, Food Ingredients, and Dietary Supplements
Nov 2012
Obtaining an FDA Investigational Device Exemption - Webinar By GlobalCompliancePanel
Nov 2012
Process Validation for Medical Devices
Nov 2012
Configuration Management and Change Control for Computer Systems
Nov 2012
Implementing Medical Device Complaint Handling Systems
Nov 2012
Design Control for Medical Devices
Nov 2012
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Nov 2012
Avoiding an FDA Warning Letter with a Strong CAPA Program
Nov 2012
Pharmaceutical Water System Sampling: Avoiding Problems by Doing It Right & The Practicality of Real-Time Release
Nov 2012
21 CFR Part 11: Complying with Part 11 Regulation - Understanding the Predicate Rule
Nov 2012
Top Ten Technology Mistakes - And How to Avoid Them
Oct 2012
Computer Systems Used in Clinical Trials
Oct 2012
21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits
Oct 2012
Anticipated Changes to the EU Medical Device Directives; 2010 Changes and What the Future Holds for Licensees - Webinar By GlobalCompliancePanel
Sep 2012
Post Market Surveillance for Medical Devices
Sep 2012
Successful 510(k) submission: Contents and Format
Sep 2012
Update on Unique Device Identifier for Device Manufacturers
Sep 2012
FMEA and Risk Management for Medical Devices
Sep 2012
Incorporating Six Sigma DMAIC into CAPA
Sep 2012
Creating Effective Master Validation Plans
Sep 2012
Key Steps to Avoid 483 Warning Letters & Remediation if you get one
Sep 2012
Site Challenges in Conducting Investigational Device Trials
Aug 2012
Management Controls Under QSR and ISO 13485 - Webinar By GlobalCompliancePanel
Aug 2012
Software Validation Planning for Executives and Managers - Webinar By GlobalCompliancePanel
Jul 2012
Software V&V Protocols and Documentation - Webinar By GlobalCompliancePanel
Jul 2012
Device Corrections and Removals
Jun 2012
Preparing for FDA Inspection and Handling the Consequences
May 2012
Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 2012
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
Off Label Product Use Discussions in Social Media
Apr 2012
Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
Apr 2012
Medical Device Risk Management Using ISO 14971
Mar 2012
Elegant Quality Assurance Practices for Device Efficacy and Efficiency Requirements
Mar 2012
Project Management To Meet CGMP Requirements
Mar 2012
Doing Business Despite Embargoes and Sanctions: OFAC Licensing
Mar 2012
Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment
Mar 2012
Advanced Methods of Root Causes Analysis for ISO 14971 Risk Reduction
Mar 2012
Quality System Approach and Risk Management for Clinical Trials
Feb 2012
Live Web Seminar Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA By compliance2go
Feb 2012
How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Feb 2012
Live Web Seminar Design Controls: What to know when it comes to FDA regulated industry? By compliance2go
Jan 2012
Application of CAPA in (Device) Sterilization – For the Non-Expert
Jan 2012
Live Web Seminar China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations By compliance2go
Jan 2012
Medical Design & Manufacturing (MD&M Online)
Dec 2011
Draft Guidance for Device Industry and FDA - Postmarket Surveillance
Dec 2011
Live webinar on Applying GMP Quality Principles To a Startup a Medical Products Manufacturing Facility From Scratch By Compliance2go
Nov 2011
Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel
Oct 2011
Does your Equipment Program Meet Current Regulatory Expectations - Webinar By GlobalCompliancePanel
Oct 2011
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems-By Howard T. Cooper
Sep 2011
Design Reviews for Efficiency and Efficacy - Webinar By ComplianceOnline
Aug 2011
Sterilization Options for Challenging Products - Webinar By ComplianceOnline
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
Advertising and Promoting FDA Regulated Products - Webinar By ComplianceOnline
Jul 2011
DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel
Jun 2011
Master Production Record Requirements - Webinar By GlobalCompliancePanel
Jun 2011
Develop and Execute the Company Software V&V Program - Webinar By GlobalCompliancePanel
Jun 2011
Sterilization Options for Challenging Products
May 2011
Patient Recruitment & Retention – Challenges & Best Practices
May 2011
Pharmaceutical and Medical Device Validation Guidance`s - Similarities and Differences - Webinar By GlobalCompliancePanel
May 2011
The GCP/ICH Obligations of Sponsors, Monitors, and Investigators - barriers and solution - Webinar By GlobalCompliancePanel
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
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements - ComplianceOnline Medical Device Training
Apr 2011
Process Validation for Medical Device Manufacturers
Apr 2011
Preparing for Pre-approval Inspections - Webinar By GlobalCompliancePanel
Apr 2011
The 510(k) Process and Risk Management
Apr 2011
FDA`s Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List - Webinar By GlobalCompliancePanel
Apr 2011
Understanding Attribute Acceptance Sampling including Z1.4 and c=0 Plans - Webinar By GlobalCompliancePanel
Apr 2011
Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel
Apr 2011
The Use and Mis-use of FMEA in Medical Device Risk Management - Webinar By GlobalCompliancePanel
Apr 2011
Change Control -- Your Company`s GMP Weak Point - Webinar By GlobalCompliancePanel
Apr 2011
Recent Major Industry CGMP Failures
Apr 2011
Controlled Substances and the Hospital Pharmacy - Webinar By GlobalCompliancePanel
Apr 2011
Understanding the Calibration Curve - Webinar By GlobalCompliancePanel
Mar 2011
A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - Webinar By GCPanel
Mar 2011
Navigating the Regulatory Environment for the Implementation of Alternative Microbiology Technologies - Webinar By GCPanel
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
Off-Label Promotion of Drugs - Regulatory Documents Explained - Webinar By GlobalCompliancePanel
Mar 2011
Design Control Explained - Medical Device Webinar
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
The Investigation System (Discovery, Planning, Root Cause Analysis, CAPA) - Webinar By GlobalCompliancePanel
Mar 2011
Food Drug & Cosmetic Act: Implementing Regulations & Major New Laws - An Overview - Webinar By GlobalCompliancePanel
Mar 2011
Complying with HIPAA Security Rules: What`s in the rules and how you can most easily prepare for compliance - Webinar By GlobalCompliancePanel
Feb 2011
Software Verification and Validation Planning and Execution
Feb 2011
Risk-Based Verification and Validation Planning to Meet U.S. FDA, ICH Q9 and ISO 14971
Feb 2011
Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel
Jan 2011
Validating Excel and Word Applications Documents - ComplianceOnline Medical Device Training
Dec 2010
Updated EU filing and registration procedures (including the new variation rules coming in to force) - ComplianceOnline Medical Device Training
Nov 2010
EU Medical Device Changing Regulatory Landscape; Changes Now and What Current Re-writes Hold for 2011-12 - ComplianceOnline Medical Device Training
Nov 2010
Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process
Nov 2010
Q4 EMT (Emerging Medical Technologies) Spotlight
Nov 2010
Robust Process Validation for Medical Devices - Webinar by GlobalCompliancePanel
Sep 2010
Validating Radiation Sterilization for medical device industries
Sep 2010
Effective Quality Process Improvement for Medical Device Firms: Don’t get caught managing process through standardized SOP’s
Sep 2010
Medical Devices in the EU: CE Mark and 93/42/EEC Directive
Sep 2010
Developing an ethylene oxide (EO) sterilization process for a product with limitations
Sep 2010
Product Risk Management - ISO 14971 and ICH Q9
Aug 2010
Understanding International Standards for Medical Devices
Aug 2010
EE Times Virtual Conference: Medical System Design
May 2010

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