Bridging User Needs & Design Requirements
1:34:11
510(k) and Substantial Equivalence: Why Do So Many Get It Wrong?
1:15:21
How to Implement and Maintain a Modern CAPA System while Avoiding Common Pitfalls
29:27
Developing a Testing Plan for Medical Device Design Verification
1:05:23
10 Things You Must Know About Updating Your Technical Files to Comply with EU MDR
1:07:42
Food Safety Culture, Frank Yiannas
1:20:22
Bridging the Gap Between Development and Regulatory Teams
1:05:20
How to Apply Risk Management Throughout the Product Lifecycle of Your Medical Device
3:50:19