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Medical Devices Events

Evolving Medical Device Regulatory Requirements and the Impact on Achieving and Maintaining CE Marking

BSI is proud to host our Medical Devices Regulatory Seminars mid to late November for medical device manufacturers, regulatory affairs and quality assurance staff. Our full-day Medical Device Seminars are focused on the European medical device regulatory and quality assurance landscape, sharing current experience, best practice and the latest expectations from the perspective of the Notified Body for CE Marking, ISO 13485 and MDSAP certification.