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Bulletproof CAPA Handling and Investigations for Medical Devices: 2 - Day In-person Seminar

7 - 8 November 2013, Boston, United States


Introduction
Course Description:
FDA's findings of Medical Device company Quality System Regulation (QSR) deficiencies in 2012 fall into four areas, of which two are especially prominent: Corrective and Preventive Action (CAPA) and Production and Process Controls (P&PC), both of which accounted for 30% of all cited deficiencies. Between January 2012 and May 2013, FDA issued 126 Medical Device Warning Letters containing noted CAPA deficiencies.
Venue

Boston, United States

Organised by
ComplianeOnline
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