Skip to main content
  • On-demand Webinar

Medical Device Single Audit Program Overview

Learn about the MDSAP requirements for certification.

Photo of doctors analyzing data

Internationally-recognized subject matter expert Mark Durivage shares his expertise on the Medical Device Single Audit Program (MDSAP) requirements for certification. During this webinar, he covers the MDSAP audit process model, how to manage the audit process, how audit nonconformances are graded, and reporting and response requirements.

Key points:

  • Identify the participating regulatory agencies, official observers and affiliate members
  • Understand the benefits of MDSAP and how it works
  • Identify and understand the MDSAP audit chapters
  • Understand nonconformance grading and audit follow-up
  • Discuss the MDSAP audit sequence


Mark Durivage, managing principal consultant, Quality Systems Compliance LLC 

Webinar date:

March 5, 2020

Medical Device Single Audit Program Overview

Get in touch

Have questions, need specifics? Let's get this conversation started.

Help and support

How can we help?