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Recorded Webinars
Carolyn Troiano | View Anytime | 4 Hours
4-Hour Virtual Seminar on FDA Trends for Computer System Validation (CSV) Compliance and Enforcement
Gina Reo | View Anytime | 60 Minutes
Developing an Environmental Monitoring Program Satisfying FDA's Listeria Monocytogenes
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)
Charles H. Paul | View Anytime | 90 Minutes
Post-Market Surveillance And Project Management Ensuring Long-term Success
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