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The transition to FDA's Quality Management System Regulation (QMSR) is Fast Approaching. Are you prepared? Join the Twin Cities Chapter and ISO working group member, @Mark Swanson, on August 14 to learn about some key updates of concern to company management, where to focus your efforts in doing updates to your processes as well as other actions/activities (training for personnel, audit/inspection management and how this could affect any submissions or responses to FDA 483 observations)

Come with your questions and concerns as the transition date (February 2, 2026) is coming quickly!!

Register today at: https://www.raps.org/events/twin-cities-chapter-in-person-event-fda-quality-management-system-regulation-qmsr--what-needs-to-be-done-dont-panicplan

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Lisa Pritchard
VP of Regulatory, Quality, Clinical and Engineering
DuVal & Associates PA
Bloomington MN
United States
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Great session, lots of good information covered. Please be sure to send out the slides - with the power outage we were not able to capture the code to get our certificate of attendance!

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Nancy Cameron RAC
Distinguished Regulatory Affairs Advisor
Medtronic, Inc. - ENTERPRISE
United States
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