Events: detail
US FDA QUALITY SYSTEM REQUIREMENTS FOR MEDICAL DEVICES (FDA Inspections ~ Is Your Quality Management System Ready?)
- Hosted by:
- Management Forum Ltd
- Speaker:
- None listed
- Starts:
- September 13, 2007 at 10:30 am
- Ends:
- September 13, 2007 at 06:00 pm
- Location:
- Rembrandt Hotel, 11 Thurloe Place, London, SW7 2RS United Kingdom
- Maps:
Description
This one day seminar will address the US FDA Quality System regulation with emphasis on FDA’s current focus. The US FDA requirements will be presented to compare and contrast with ISO13485 and ISO14971 Risk Management. Actual FDA Warning Letter examples will be used to illustrate key points. In addition, the FDA inspection process will be explained with advice on how to prepare your company to respond to 483s and Warning Letters.
- Registration required:
- Yes
- Free:
- No
Additional information
£510 + VAT
For more information
- Contact person:
- Management Forum
- Phone:
- 01483 730008
- Email:
- registrations [ at ] management-forum.co.uk
- Website:
- US FDA QUALITY SYSTEM REQUIREMENTS FOR MEDICAL DEVICES (FDA Inspections ~ Is Your Quality Management System Ready?)
