Automatic language translation

Our website uses an automatic service to translate our content into different languages. These translations should be used as a guide only.

Federal Register Notice - Medical Device ISO 13485:2003 Voluntary Audit Report Pilot Program; Termination of Pilot Program; Announcement of the Medical Device Single Audit Program Operational Phase

17 December 2015

US Federal Register notice regarding MDSAP moving into an operational status from a pilot program:

Medical Device ISO 13485:2003 Voluntary Audit Report Pilot Program; Termination of Pilot Program; Announcement of the Medical Device Single Audit Program Operational Phase