Class I Medical Device Manufacturers Need an established QMS Under the New MDR
Swedish MedTech Regulatory Summit Presentation
We recently had the pleasure of attending the Swedish MedTech Regulatory Summit in Stockholm on March 30th — an annual recurring conference focused on the latest developments in the medical technology regulatory framework. It was a fantastic opportunity to learn about the industry’s latest trends and we were delighted to connect with so many delegates from other medical device businesses as well as Swedish Medtech network partners.
One of the highlights of the event was our very own Sofie Petersson, who was a speaker at the conference. Sofie is MedQdoc’s Senior Quality and Regulatory Advisor and Acting Quality and Regulatory Manager as well as Management Representative and PRRC in the medical device industry.
Sofie’s presentation focused on QMS digitisation and the challenges faced by medical device businesses when it comes to choosing and implementing a QMS. With real-world case studies and examples, Sofie demonstrated how MedQdoc has helped businesses improve operational efficiency, reduce errors, enhance traceability and improve regulatory compliance. We were delighted to share our expertise with the wider MedTech community and to see the positive response from the audience.
MedQdoc is used across the medical device industry
