Events
US FDA Quality Systems and Medical Device Requirements
10-11 December 2009The Rembrandt Hotel
London, UK
Website: www.management-forum.co.uk
This meeting will help delegates to understand the US FDA Medical Device Quality System Regulation 21 CFR Part 820 and learn how to successfully apply the regulations. It will provide information about management controls, design controls, production and process controls and corrective and preventative action. It will help delegates plan how to align US FDA quality system requirements with ISO 14971 Risk Management, prepare for US FDA inspections; know how to respond to FDA 483s and warning letters and understand complaint handling, vigilance and postmarket surveillance.
