Regulatory Documents Explained - DHF, DMR, DHR and TF
1:05:37
Managing the Medical Device Supply Chain
58:34
Documentation Deconstructed: Understanding the Technical file
1:02:57
FDA Quality Systems Regulation Requirements - Regulatory Documents Explained
1:10:24
FDA Requirements for Device Labeling
1:19:59
Requirements Contents and Options : The 510k Submission
1:08:18
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
1:12:45
The New Medical Device Regulation (MDR) - Webinar
17:07