Season´s Greatings! And best wishes for the New Year!
Even this year QAdvis refrain from Christmas gifts and choose to contribute to better health by ...
Welcome Irene Sebastianutto
We are very glad to welcome two new consultants to our team. Irene Sebastianutto PhD, native ...
QAdvis congratulate EXINI Diagnostics AB for achieving their MDR-certificate
QAdvis want to congratulate one of our customers, EXINI Diagnostics AB, for achieving their ...
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 ...