QAdvis congratulate EXINI Diagnostics AB for achieving their MDR-certificate
QAdvis want to congratulate one of our customers, EXINI Diagnostics AB, for achieving their ...
Author Aurevia:
United Kingdom Responsible Person
We are delighted to offer our professional services and to support you with successful post-Brexit ...
Accelerating Innovation & Streamlining Compliance for Medical Devices Engineering
QAdvis is pleased to participate in an exclusive webinar designed for the Medical Device ...
Person Responsible for Regulatory Compliance
One important new requirement in both MDR and IVDR is to have an assigned and dedicated Person ...
News in medical technology
The new legislation on medical devices in the EU, MDR and IVDR has greatly influenced the need for ...
What is Eudamed?
Eudamed is an IT system developed by the EC to implement medical device and in vitro diagnostic ...
IDL Biotech has chosen QAdvis for regulatory guidance and support
QAdvis has signed an agreement with IDL Biotech. We are proud to be a part of this exciting ...
QAdvis News #3 – 2020
Less than 9 months to go until Date of Application (DoA) for MDR, 26 May 2021. But is the DoA for ...
Update on situation with Covid-19
The ongoing situation with Covid-19, with the extended time range on recommendations to work from ...