QAdvis is a solution-oriented trusted service provider for the medical device and in vitro diagnostic device sector. To enable and maintain global market access, we can with high level of knowhow and expertise within quality management and regulatory affairs support your company to be in compliance with applicable regulations and requirements. QAdvis was founded in 2013 and is based in Sweden. We are certified according to ISO 13485:2016.
This Christmas we save children’s lives
We at QAdvis wish all of our customers and partners a Merry Christmas and a Happy New Year! This year QAdvis refrains from sending Christmas gifts but instead chooses to contribute to the important work of UNICEF in Ukraine.
Proposed changes of MDR transition times
EU Commission is proposing elements of a bridging measure for MDD certificates that expire pending MDR conformity assessment A Commission proposal for bridging measures for certificates that expire pending MDR conformity assessment was on the agenda for the EPSCO meeting on December 9, 2022. The proposal suggests an extension of the transition time for legacy […]
Internship at QAdvis
We are happy to welcome Sneha Bangalore to QAdvis. Sneha has been hired via Jobbsprånget as an intern and will be a part of our teams in both Stockholm and Lund. She has recently finished her master’s degree in applied biotechnology from Uppsala University. During her master she has among other things studied molecular biotechnology, […]
Career at QAdvis
To our offices in Lund and Stockholm we are now looking for new colleges that will work together with us and our clients as Quality & Regulatory consultant within the Medical Device and In Vitro Diagnostic medical device industry. Read more here
Welcome Noomi
We are very pleased to announce the joining of our new colleague Noomi Altgärde and extend a warm welcome to the QA&RA consultant team at QAdvis! Noomi has a PhD in Bioscience and a long background from working with medical devices in the development phase, with a focus on quality assurance and regulatory affairs. Her […]