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# MDSAP Participants Sought
- URL: https://www.fdaweb.com/mdsap-participants-sought/
- Published: 2016-09-08T12:00:00.000Z
- Updated: 2026-09-14T21:30:22.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5136750

The FDA Medical Device Single Audit Program (MDSAP) Regulatory Authority Council is inviting medical device manufacturers to participate in the regulatory single audit program. An online [invitation](http://www.fda.gov/downloads/MedicalDevices/InternationalPrograms/MDSAPPilot/UCM519565/pdf?ref=fdaweb.com) says an MDSAP pilot opened 1/1/14 and is the implementation of an International Medical Device Regulators Forum MDSAP initiative. The transition to full program implementation is expected to begin 1/1/17.

Countries represented in the program are Australia, Brazil, Canada, Japan, and the U.S.

“MDSAP enables medical device manufacturers to contract with an MDSAP authorized auditing organization to conduct a single audit against the relevant medical device regulatory requirements of all fully participating regulatory authorities,” the notice says.