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Partner Event: BSI Roadshow - EU Regulatory Requirements for Medical Devices
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Partner Event: BSI Roadshow - EU Regulatory Requirements for Medical Devices

BSI's free half-day event will provide the latest update on topical changes proposed on European medical device regulations, ISO 13485, MDSAP and Unannounced Visit experience. Key technical sessions will also review current expectations and best practices for CE Marking clinical data evaluation and common problems with technical documentation suppo

3/10/2015
When: 3/10/2015
8:30 AM
Where: Hilton St. Petersburg Carillon Park
950 Lake Carillon Drive
St. Petersburg, Florida  33716
United States

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BSI is supporting medical device manufacturer regulatory affairs and quality assurance professionals through our second annual Mini-Roadshow program.  Our free half-day event will provide the latest update on topical changes proposed on European medical device regulations, ISO 13485, MDSAP and Unannounced Visit experience.  Key technical sessions will also review current expectations and best practices for CE Marking clinical data evaluation and common problems with technical documentation supporting compliance with EU medical devices directives.  We invite you join the BSI experts to discuss critical topics and receive timely insights from the perspective of the leading Notified Body for CE Marking of medical device, ISO 13485 registrar, and the first national standards body.

 

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