We strengthen our team.

QAdvis is happy to welcome Marie to our growing team of experienced quality and regulatory consultants. Marie has an extensive background in regulatory compliance within the medical device sector. She has previously worked at the Swedish Medical Products Agency as an investigator of post market surveillance and navigated complex vigilance reporting cases, including CAPA and FSCA. She has broad experience in risk assessments for both medical devices and In-Vitro diagnostic devices. This strategic expansion is a testament to our commitment to continuous growth and to meet the current and future quality and regulatory requirements throughout the development, market launch and the post market surveillance of medical devices.

If you want to learn more about Marie and her experiences and how QAdvis can contribute to your business, contact us at info@qadvis.com or call us at + 46 86 21 01 05.