QAdvis wishes our customers & partners a Merry Christmas and Happy New Year!
We refrain from physical christmas gifts and choose to support the Swedish Childhood Cancer ...
Author Aurevia:
October has been a busy month for us here at QAdvis
This week, Robert Ginsberg, QAdvis’s Chairman of the Board, was speaking at RMD in Brussels, our ...
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 ...
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 ...