EU Medical Device Regulation (MDR)

EU Medical Device Regulation (MDR)

The Medical Device Directive (MDD) was replaced by the Medical Device Regulation (MDR 2017/745) in May 2021. Medical devices with a valid MDD EC Notified Body certificate may during a transition period still be placed on the market until May 2024.

The new regulation will have a great impact on all medical device actors, throughout the lifecycle of the devices, with stricter requirements on both products and on manufacturers’ Quality Management Systems.

In this course you will get a basic understanding of the new requirements to help you prioritize and succeed with the MDR transfer.

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Information

When: Fri, 30 Sep 2022 09:00 to 16:00
Where: Medicon Village
Organizer: QAdvis AB
Language: Swedish
Price: 6900 SEK
VAT excluded

Registration

Link to website or email address
Application deadline

Category

Seminarium/utbildning

Contact information

Hermine Redl
+46 8 621 01 05
academy@qadvis.com
https://www.qadvis.com/portfolio-item/eu-medical-device-regulation-mdr-2/