FULLY BOOKED

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 event which includes 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 details, please see the attached programme.

To register for this event, please complete the online booking form below.