The Medicines and Healthcare products Agency (MHRA) launched a public consultation on the EC proposed regulation on medical devices to better identify and evaluate the full implications of the changes to the various stakeholders. This consultation will help the UK to negotiate with the other EU Member States and the European Parliament.

This consultation closed on 21st January 2013.
We are happy to share our input to the consultation. You can read here  COCIR Contribution to MHRA Consultation on draft MD Regulation.