Our collaboration with Swedish Medtech has been successful since 2018 and we are proud to participate in the Swedish Medtech Regulatory Summit 2021. Senior Quality and Regulatory consultant Anna-Karin Areskog will make a presentation on the latest status regarding IVDR implementation.
QAdvis consultant will during the spring be part in several presentations in the MedTech4Health program to improve knowledge regarding quality and regulatory for medical device and IVD manufacturers.
The program is conducted in cooperation with Swedish Medtech and has more than 100 participants from different startups and small innovative companies within Sweden. QAdvis is proud to be part of this series of presentations, Senior Quality och Regulatory consultant Emma Axelsson is one of many, to inspire to early starting to include quality and regulatory issues in the development process.