The course covers the requirements of the Medical Device Regulatory Standard ISO 13485 and the regulatory framework and documentation required to market a medical device.Those attending will get an understanding of the requirements and documentation required to market and maintain compliance for medical devices in the market place. There are tutorials on the Directives, the regulatory system, the marketing of a device and the ISO 13485 Medical Device Standard. Added to this there is an introduction to risk management and the vigilance system. The course is interactive with many practical exercises and discussions.
Good Manufacturing Practice Medical Devices
1 November 2012, Reading, United Kingdom
Introduction
Venue
RSSL Pharma Training
RSSL Pharma Training, Whiteknights Road, Reading, RG6 6BZ, United Kingdom
Useful links
Organised by
RSSL Pharma Training
Contact information
Mrs Rachel Horton
Reading Scientific Services Ltd, The Reading Science Centre, Whiteknights Campus, Reading, RG6 6LA, United Kingdom
0118 9184024
Contact us by email
Reading Scientific Services Ltd, The Reading Science Centre, Whiteknights Campus, Reading, RG6 6LA, United Kingdom
0118 9184024
Contact us by email
Search
Advertisement
Spotlight
Explore
Membership
