What to do during recalls, removals, and market corrections
1:05:37
Managing the Medical Device Supply Chain
1:08:18
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
1:10:24
FDA Requirements for Device Labeling
1:03:26
Ensure data integrity and subject safety in clinical research
1:18:50
Statistical Concepts of Process Validation
1:29:36
Understanding Attribute Acceptance Sampling including Z1 4 and c=0 Plans
1:13:42
Medical Device Adverse Event Reporting in EU, US and Canada
1:08:12