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Medical devices

In this webinar, we will cover the key points to be aware of during your migration to the MDR, help you prepare for the date of application, which is May 26, 2021, and outline the expectations and requirements to be met. Key points covered will include: classification rules, technical documentation, economic operators, and post market surveillance.

Following the webinar, you will be better prepared to meet the increased requirements that have been placed on medical device manufactures. You will gain an understanding of your next steps, whether it is additional MDR transition training, or what to discuss with your notified body.

Medical Device Regulation – MDR Transition Update

Download the slides for the March 12, 2021 webinar

"Medical Device Regulation – MDR Transition Update" webinar presentation materials

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