On 28 January 2014, LRQA are hosting 'Preparing for change in 2014 . . .' an LRQA medical directives update seminar for all medical device and in-vitro diagnostic device manufacturers on the proposed new regulations that will replace the current directives.
On the 24 September 2013 the European Commission Implemented the Regulation (EU) No 920/2013 and the Recommendation (2013/473/EU) with immediate effect. These cover some of the requirements in the proposed regulations published by the European Commission on 26 September 2012, which will be implemented in the forthcoming years.
The changes have started now, so LRQA have identified what you need to prepare in 2014 to help you meet the new regulatory requirements.
We are hosting this update seminar to provide all medical device manufacturers with detailed knowledge and understanding on the proposed changes to help them start planning and working towards implementing the recommendations and the new regulations.
Who should attend?
Those who are responsible for ensuring your medical or in vitro diagnostic device meets regulatory requirements:
LRQA clients - £195
Non LRQA clients - £250