Training

The following pages provide resources to support Regulatory Authorities (RA), Auditing Organizations (AO) and medical device manufacturers understand and participate in the MDSAP.

In a secure area, the MDSAP also maintain a suite of other resources that support the program, including training modules for recognized MDSAP AOs, and RAs seeking membership in the program. To request access to these resources, please contact us.

MDSAP Education Modules (CDRH Learn)

To inform the medical device manufacturing community about MDSAP, the U.S. Food and Drug Administration developed 10 medical device education modules.

Other Resources

Information pertaining to MDSAP competence and training produced by the International Medical Device Regulators Forum (IMDRF).