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Join your quality and regulatory colleagues from the ASQ Biomedical Northern California Discussion Group and the RAPS San Francisco Bay Area Chapter for a lively and informative one-day workshop on documenting key quality and regulatory processes. Experts use a mythical medical device to demonstrate by example how to prepare key documentation in the following areas:
**Risk Management**
Corrective and Preventive Actions (CAPA)**
Usability Engineering **
Essential Requirements **
Technical Files **For more information and to register please click on website provided.
Web site: http://www.raps.org/personifyebusiness/Bookstore/ProductDetail/tabid/55/Default.aspx?ProductId=6298 |
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All dates, locations, times and activities are subject to change. |
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