Clinical research – increasing hope for more patients
To keep up with the development of new pharmaceuticals and medical devices, more clinical studies ...
Author Aurevia:
Thanks to Swedish Medtech Regulatory Summit
Last week we were present at the Swedish Medtech Regulatory Summit. A big thank you to Swedish ...
… with BSI regarding MDR-Application Process
MDR Application Process – What do you need to know? QAdvis have invited Magnus Olla from BSI in ...
Extension of the MDR transitional period and removal of the “sell off” periods
European commission has now official published the Q&A on practical aspects related to the ...
Come and Meet Us at the Regulatory Summit on March 30th
We are present at Swedish Medtech’s Regulatory Summit on March 30th. Meet us here if you want to ...
Welcome Linda Lindberg!
We are happy to announce that QAdvis has a new consultant in our team, a warm welcome to Linda ...
QAdvis Collaboration with Swedish Medtech Continues in 2023
QAdvis will remain as a Swedish Medtech networking partner in 2023 and together we are offering ...
Voting Complete – extension of MDR transition times and removal of sell-off period for devices from MDR and IVDR
The EU Parliament has adopted the MDR amendment proposal, February 16th, and removed the sell-off ...
The 7th EAAR Annual Conference on the New Medical Device Regulations
Welcome 2-3 February in Brussels, Belgium to listen to Robert Ginsberg, Nils-Åke Lindberg and many ...