Recorded Webinars
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 | 60 Minutes
Device Changes, FDA Changes, and the 510(k)
John C. Fetzer | View Anytime | 60 Minutes
How to Deal with Bad Results Under GLP
John C. Fetzer | View Anytime | 60 Minutes
HPLC Analytical Method Development and Validation
John C. Fetzer | View Anytime | 60 Minutes
Analytical Method Validation Under Good Laboratory Practices
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