TÜV SÜD’s designation under the EU’s in vitro diagnostic regulation (IVDR) is still ongoing and is expected to be completed by the end of the summer. To this date there are no NBs designated under the IVDR yet.

TÜV SÜD has a large capacity and the NB claims to have over 500 medical experts, engineers and doctors around the globe. It has been suggested that TÜV SÜD accounts for a third of all EU medtech notified body activity.

Current predictions are that there could be up to 10 notified body designations by the end of this year in total under the two Regulations, but that this figure is not likely to rise above 20 by 26 May 2020, when the MDR fully applies.

Should you want to discuss this more in depth with one of our consultants, please do not hesitate to get in touch with us.

QARAD B.V.B.A.

ISO 13485 Certified

Follow us on:

Quicklinks

Website by Contents by Qarad Terms and conditions  Privacy policy  Cookie policy 
Close

Attention!

This website uses cookies to enhance your surfing experience.
Certain webfunctions rely on the usage of these cookies.
If you want more information regarding our cookie policy, you may visit this link.