21 CFR Part 820

How the Document Hierarchy Works in a Life Science Environment – With Example [Video]

The Reason Why Organizations Resist Approving Design Documents [Video]

ISO 13485:2016: The Biggest Mistake to Avoid with Dealing with Design Controls [Video]

Medical Device Production and the Importance of the Quality Plan [Video]

How to Handle Medical Device Non-Conformances [Video]

The Main Deliverables of a Validation Master Plan (VMP) [Video]

All You Need to Know About Quality Policies – ISO 13485 : 2016 [Video]

How the FDA Audit Personnel Controls – 820.70(d) [Video]

The Difference Between ISO 13485 and ISO 9001 [Video]

Your 1 Minute Guide to Incoming Material Inspection – 21 CFR Part 820.80(b) [Video]