Medical Devices webinars
Covers medical device quality and design compliance, including design controls, ISO 14971 risk management, IEC 62304 software, supplier controls and CAPA.
1live webinars in the next 2 weeks
26recorded Medical Devices sessions
60–90minutes each, with live Q&A
Upcoming Medical Devices webinars
LIVE
Batch Record Review and Product Release
Danielle DeLucy
60 minView webinar →
No live webinars on this topic right nowSee the on-demand recordings, or ask us to schedule one.
ON-DEMAND
Medical Device Hazard analysis following ISO 14971
Edwin Waldbusser
60 minView webinar →
ON-DEMAND
How to Write Procedures to Avoid Human Errors
Ginette M. Collazo
90 minView webinar →
ON-DEMAND
Human Error Reduction Techniques for Floor Supervisors
Ginette M. Collazo
90 minView webinar →
ON-DEMAND
Project Management for Non-Project Managers - Scheduling your Project
Charles H. Paul
90 minView webinar →
ON-DEMAND
Impact Assessments For Supplier Change Notices
Alan M Golden
60 minView webinar →
ON-DEMAND
Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration
Jose Ignacio Mora
60 minView webinar →
ON-DEMAND
Impact of machine learning in pre-clinical research and regulatory compliance
ON-DEMAND
Design Control for Medical Devices and Combination Products
Alan M Golden
60 minView webinar →
ON-DEMAND
Successful Supplier Audits
Danielle DeLucy
60 minView webinar →
ON-DEMAND
Risk Assessment for Medical Devices
Charles H. Paul
60 minView webinar →
ON-DEMAND
Project Management for Non-Project Managers
Charles H. Paul
60 minView webinar →
ON-DEMAND
Implementing a Change Control Quality System Successfully
Danielle DeLucy
60 minView webinar →
ON-DEMAND
Human Error Reduction in GMP Related Environments
Ginette M. Collazo
60 minView webinar →
ON-DEMAND
Human Error Reduction in GMP Manufacturing Environments for Floor Supervisors
Ginette M. Collazo
90 minView webinar →
ON-DEMAND
Medical Device Software Per IEC 62304
Jose Ignacio Mora
60 minView webinar →
ON-DEMAND
Software Validation for the New FDA Inspections
Edwin Waldbusser
60 minView webinar →
ON-DEMAND
Proper Execution of Annual Product Reviews
Danielle DeLucy
60 minView webinar →
ON-DEMAND
Developing an Effective CAPA Management and Root Cause Analysis System
Danielle DeLucy
60 minView webinar →
ON-DEMAND
Risk Management Under ISO 14971 Integrating Concepts From IEC 62304 and ANSI 62366
Don Hurd
75 minView webinar →
ON-DEMAND
Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
Jose Ignacio Mora
90 minView webinar →
ON-DEMAND
Understand CERT Findings and What Your Organization Should Be Monitoring
Pamela Joslin
60 minView webinar →
ON-DEMAND
FDAs Final Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List
David R. Dills
60 minView webinar →
ON-DEMAND
FDA Regulations for Pharmaceutical Good Manufacturing Practice (GMP)
Loren Gelber
90 minView webinar →
ON-DEMAND
Best practices for purchasing and supplier controls in the medical device industry
Jeff Kasoff
60 minView webinar →
ON-DEMAND
Gaining And Re-Establishing Control Of Your Cleanroom
Joy McElroy
60 minView webinar →
ON-DEMAND
Preparing And Investigating Oos/Oot Results In A Regulated Environment
Danielle DeLucy
60 minView webinar →
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