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2019 EU In Vitro Diagnostic Regulation Workshop

April 30

BSI is proud to host our inaugural EU In Vitro Diagnostic Regulation (IVDR) Workshop for the in vitro diagnostic device manufacturer regulatory affairs, quality assurance and related consulting community.

Our unique EU IVDR Workshop event is exclusively focused on addressing the European IVDR. BSI will be sharing our current experiences, best practice and expectations from the perspective of the leading global medical device Notified Body, ISO 13485 registrar, MDSAP Auditing Organization and world’s first national standards body.


April 30


San Jose, CA