GMED North America is hosting a RAPS DC/Baltimore Chapter in-person event on June 5, 2025, between 4:30 and 7:00 p.m. (EST) focused on unlocking the potential of the Medical Device Single Audit Program (MDSAP), a program that allows for a single regulatory audit of a medical device manufacturer’s quality management system to satisfy the requirements of multiple regulatory jurisdictions.
The agenda includes presentations from our experts Ehab Amen, Certification Division Director, and Pascal Bisson, Lead Auditor, Product Reviewer and MDSAP coordinator, who will cover MDSAP requirements, the audit process, tips for successful implementation, and the added value of this program to ensure patient safety.
We will also listen to a case study presentation from a medical device manufacturer who has successfully implemented MDSAP.
During this event, you will have the opportunity to network with peers and industry experts, gain practical insights, ask questions, and connect with professionals dedicated to advancing the medical device industry.
Don’t miss this chance to enhance your understanding of MDSAP and its benefits. We look forward to seeing you there!
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