This webinar will help orthopedic device companies identify the critical elements required for MDSAP and understand the MDSAP process and its correlation with ISO, MDR and the 510(k) process.
The Medical Device Single Audit Program (MDSAP) is the single audit program that covers the regulations of Australia, Brazil, Canada, Japan and the United States. These regulators use MDSAP to verify compliance to the quality systems of their national regulations and ISO 13485. The process is task-based and follows a prescribed audit flow, minimizing business disruptions and optimizing time and resources.
Date/Time: July 27, 2021 2:00 pm - 3:00 pm EST
For more information, please contact:
Victoria Leo
Marketing Specialist
t: +1 201 508 3000