Becoming Compliant with the MDRs, A Real Life Case Study

Tue. February 5| 1:30 PM - 2:15 PM | Tech Theater, Booth 637, Hall E

Audience Level: All

Show: General

Track: Tech Theater

Focus: 3D Printing, Contract Manufacturing, Design & Product Development, F&B Packaging, Injection Molding, Labels & Labelling, Materials, Robotics & Automation

The new Medical Device Regulations (MDRs) become enforceable May 2022. After that, all new devices set for market in the European market will have to demonstrate compliance with ISO 10993, even if the device has been on the market for years. This presentation will walk through a real life example of bringing a device that has been on the market in Europe into compliance with the ISO 10993 and the new MDRs.


Matthew Jorgensen

Matthew Jorgensen

Chemistry and Material Scientist

Nelson Laboratories

Role: Speaker