Medical Device Single Audit Program (MDSAP)

The Medical Device Single Audit Program – or MDSAP – allows a single regulatory audit of a medical device manufacturer’s quality management system to satisfy the requirements of multiple regulatory authorities.

These include the Regulatory Authorities for: 1) Australia, 2) Brazil, 3) Canada, 4) Japan and 5) USA.

Details of services offered coming soon.

Contact us today if you require help with updating your Quality Management System to align with MDSAP requirements.