10 Steps to Preparing Your 510(k) Submission (and How to Avoid the Common Pitfalls)
1:01:46
How to Avoid Common Problems with your Design, Risk, and Validation Documentation
1:05:20
How to Apply Risk Management Throughout the Product Lifecycle of Your Medical Device
1:08:44
Cybersecurity Webinar - Learn what the FDA wants in your 510(k)
2:59:15
FDA Webinar on the Food Traceability Final Rule
1:25:04
Complaint Handling: How to Avoid the #3 Most Cited Reason for 483 Observations
1:05:23
10 Things You Must Know About Updating Your Technical Files to Comply with EU MDR
1:34:11
510(k) and Substantial Equivalence: Why Do So Many Get It Wrong?
1:24:09