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Recorded Webinars
Gina Reo | View Anytime | 60 Minutes
Developing an Environmental Monitoring Program Satisfying FDA's Listeria Monocytogenes
Charles H. Paul | View Anytime | 90 Minutes
Project Management for Non-Project Managers - How to Communicate Project Actions and Progress - Conducting Effective Project Review Meetings
Charles H. Paul | View Anytime | 90 Minutes
Training Strategies To Reduce Human Error In Drug Manufacturing
John E Lincoln | View Anytime | 3 Hours
3-Hour Virtual Seminar on Master Validation Plan - The Unwritten Requirements
John E Lincoln | View Anytime | 90 Minutes
Design History Files (DHF), Device Master Records (DMR), Device History Records (DHR), Technical Documentation Files - The US FDA and EU MDR Requirements
John E Lincoln | View Anytime | 90 Minutes
Device Changes, FDA Changes, and the 510(k)
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