Evaluating, Monitoring & Selecting Suppliers in the Medical Device Industry
1:03:55
Supplier Risk Management
21:41
Post-market surveillance as a medical device requirement in the EU
1:07:19
Supplier Evaluation & Assessment How to Meet FDA QSR & ISO 13485 Requirements
24:52
The Most Useful Thing AI Has Done
21:10
How to register a Medical Device with FDA? (510k, PMA, de Novo...)
13:11
ISO 13485: What You Need to Know to Build a Quality Management Systems for Medical Devices
1:05:20
How to Apply Risk Management Throughout the Product Lifecycle of Your Medical Device
26:47