BSI to hold medical device regulatory seminars next month

The full-day seminars are focussed 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.



The seminars will also provide an opportunity to meet with a panel of experts and network with colleagues from the medical device regulatory affairs/quality assurance community to discuss critical updates and receive valuable insight
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