Risk Management is traditionally an area of weakness for most companies and frequently a failure mode and effects analysis (FMEA) is the last item that is completed for the Technical File. Greater emphasis is now being given to this area - so much so it is now a theme that is being introduced throughout medical device standards. This free 1 day workshop (including several interactive workshops), run by experts in the field, will cover all the key issues that will enable you to introduce and maintain an effective Risk Management system for your company. For further detail and to register for this event, please click on the link below: http://www.medilinkem.com/web/MEDILINK/showevents.cfm?id=485
BioCity, Pennyfoot Street, Nottingham, NG1 1GF
Wed 17th Feb 2010, 09:00 to 00:30
This is a Member Event.
For all enquiries use the contact information provided above.