How to Implement and Maintain a Modern CAPA System while Avoiding Common Pitfalls
1:29:31
Refuse to Accept & Additional Information Request: Avoiding Problems with Medical Device Submissions
1:20:11
Preparing Your Technical Documentation under MDR: Proven Tips & Techniques
1:28:05
Beyond Design Controls 101: Following the Regulation vs. Understanding its Intent
46:56
Avoid Death by CAPA: The Modern Approach to Quality Event Management
58:32
Practical Guide to Cybersecurity and SBOM Management for FDA Approval
1:30:28
Post-Market Surveillance for Medical Devices & Combination Products
1:05:23
10 Things You Must Know About Updating Your Technical Files to Comply with EU MDR
1:09:23