Finally released – Guideline for medical device SW i EU
We think that many of you have waited for the guideline for medical device SW in EU! “Guidance on ...
Author Aurevia:
The 4th EAAR Annual Conference on New Medical Device Regulations
Robert Ginsberg, Chairman of the board at QAdvis and board member of European Association of ...
Strengthening our QA and RA team
We welcome Caroline Ehrenborg MSc who has just started as a QA&RA consultant. She will be a ...
New Swelife-ATMP regulatory guide
Swelife-ATMP is a project that provides expertise and support for Advanced Therapy Medicinal ...
Online course – Technical Documentation for medical devices 26 May, 2020
Our services include: • Quality management support • System development • Clinical evaluation • ...
2-day course – Risk Management for medical devices 9-10 June, Stockholm
Our services include: • Quality management support • System development • Clinical evaluation • ...
International Medical Devices Exihibition (CMEF) 2019 on 11–13 July.
QAdvis EAR Manager, Bing Wu, will visit the 25th China (Shanghai) International Medical Devices ...
Calmark Sweden AB signs agreement for consulting services for clinical studies
Calmark Sweden AB has today signed an agreement with Scandinavian CRO, a Clinical Research ...
Lumito has chosen QAdvis to support them in the CE-marking
QAdvis has signed agreement with Lumito, developers of imaging techniques for both tissue in living ...