The Swedish Medtech Regulatory Summit is just around the corner — taking place on March 12th at Hilton Slussen in Stockholm. We’re proud to share that our Senior Principal Consultant, Cecilia Emanuelsson, will be one of the speakers at this year’s conference.
Cecilia’s session will provide an overview of the regulatory requirements for clinical evaluation of Class I medical devices. With a deep knowledge of medical devices and a strong focus on patient safety from a clinical perspective, Cecilia will be sharing her expertise on MDR compliance — offering clear guidance and concrete, real world examples to help manufacturers navigate current regulatory expectations.
We look forward to engaging discussions with the medtech community — and we hope to see you there!
Do you need quality or regulatory support? Our team of experts can support you throughout the entire lifecycle of your medical device or in vitro diagnostic device.