ISO 13485:2016

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]

Your 1 Minute Guide to Line Clearance in a GMP Production Environment [Video]

Your 2 Minute Guide to Specification, Alert and Action Limits – 820.70(a) [Video]

Your Two Minute Guide to Unique Device Identification (UDI) [Video]