1:11:27

Purchasing and Supplier Controls in the Medical Device Industry

1:10:24

FDA Requirements for Device Labeling

1:06:19

What to do during recalls, removals, and market corrections

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

1:28:00

Process Validation Procedure for Medical Device Manufacturers

1:09:52

Medical Device Complaint Handling Systems

1:13:42

Medical Device Adverse Event Reporting in EU, US and Canada