MDSAP Certification: Readiness Webinar
Thu, Apr 30
|Zoom
The Medical Device Single Audit Program (MDSAP) offers a pathway for streamlined regulatory oversight, but achieving certification requires a well-integrated quality system. Join our upcoming webinar focused on MDSAP Certification Readiness.
Time & Location
Apr 30, 2026, 11:00 AM – 12:00 PM PDT
Zoom
About the event
As global regulatory expectations continue to evolve—and with FDA’s Quality Management System Regulation (QMSR) now in effect—many MedTech companies are taking a closer look at how their quality systems align with both global and U.S. regulatory expectations.
The Medical Device Single Audit Program (MDSAP) offers a pathway for streamlined regulatory oversight across multiple jurisdictions—but achieving certification requires a mature, well-integrated quality system aligned with ISO 13485 principles and risk-based decision making.
Join Jennifer Mascioli-Tudor, CEO, JMT Compliance Consulting, for an upcoming webinar focused on MDSAP Certification Readiness, where we will discuss how organizations can strengthen their quality systems to support both MDSAP certification and ongoing QMSR compliance.
This session is designed for quality, regulatory, and MedTech professionals responsible for preparing their organizations for MDSAP certification, QMSR alignment, and global regulatory inspections.