The Detectivio Journey, from Idea to MedTech Product
The beginning of a journey – The winding road from idea to product for a high-tech medical device ...
Our Due Diligence consultants are ready to support you
A well performed due diligence process is challenging but crucial in any merger and acquisition ...
QAdvis News #4 – 2020
Get ready for the new regulatory landscape in the United Kingdom – start with appointing a UK ...
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 (PRRC)
One important new requirement in both MDR and IVDR is to have an assigned and dedicated Person ...