Don Rackham

Purchasing Controls for Medical Device Companies (21 CFR Part 820.50) [Video]

Your 1 Minute Guide to the NCR Process [Video]

6 Key Elements Your Record Management System Needs [Video]

Do You Know the Various Time Points for Stability Studies? [Video]

The Two Different Approaches to Internal Quality Audits

ISO 13485:2016 – Keep the Quality Agreement Separate to the Supplier Agreement [Video]

Medical Device Reporting Timelines for the US

The Importance of Allowing Adequate Time for Design and Development Inputs | ISO 13485

3 Categories of Design and Development Inputs | ISO 13485

Overview: Design and Development Inputs | ISO 13485