Internationally-recognized subject matter expert Mark Durivage will share his expertise on the MDSAP (Medical Device Single Audit Program) requirements for certification. During this webinar, he will cover the MDSAP audit process model, how to manage the audit process, how audit nonconformances are graded, and reporting and response requirements.
Upon completion of this webinar, the participant will be able to:
•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
SCHEDULE A DEMO