Medical Device Single Audit Program (MDSAP) Frequently Asked Questions

Medical Device Single Audit Program (MDSAP)
Certified once, recognized globally

Medical Device Single Audit Program (MDSAP) Frequently Asked QuestionsThe MDSAP is a global, harmonized approach to auditing and monitoring the manufacturing of medical devices while supporting the development of a worldwide initiative of countries dedicated to pooling resources to improve the safety of medical devices. Download now and find out answers to the most frequently asked questions around the MDSAP, including:

  • What is the MDSAP Pilot Program and who should use it?
  • What are the benefits?
  • Will there be additional requirements for the manufacturer?
  • How do manufacturers currently holding ISO 13485 certification under the CMDCAS program transition to the MDSAP program?