Content relating to Medical Devices
Webinar
The ABC’s Of Medical Device Single Audit Program (MDSAP)
The Medical Device Single Audit Program (MDSAP) was created by the International Medical Device Regulators Forum (IMDRF) to enable audits that encompass ISO 13485 as well as the regulatory requirements from the United States, Canada, Australia, Brazil and Japan.
Blog
8 Factors To Prepare For Your MDSAP Audit
The Medical Device Single Audit Program, or MDSAP, is a program that allows medical device manufacturers to be audited once for compliance with the ISO 13485 standard AND regulatory requirements of participating countries.