Finland’s Eurofins Becomes EU’s 11th Notified Body Designated Under the IVDR
The number of notified bodies designated under the IVD Regulation has now crept up to 11 as the first Finnish designation is announced.
You may also be interested in...
Every designation of a notified body under the Medical Device and IVD Regulations has been greeted with fanfare given the historic pressure for more testing capacity. There may have been a shift in timelines, but IVD manufacturers still urgently need to engage with a certified testing body.
Work related to the European Commission’s promise to assess the impact of the Medical Device Regulation, including its impact on innovation, is starting to take shape.
Medtech developers have just over a month to apply for the pilot phase of a program offering regulatory and practical support to accelerate innovative product access to the UK NHS.