Download ‘MDR Insights’ – Exclusive to Global Access Attendees

Firstly, we are delighted that you have visited our virtual stand at the 2020 Global Access event hosted by Irish Medtech.

We have created a brief e-book that looks at some of the most commonly asked questions that we have received about MDR.

Acorn Regulatory is working with companies all around the world helping them to prepare for the new MDR and IVDR.  If you would like to talk to us about how we can assist your company, you can contact us by clicking here.

Our MDR Insights guide looks at the following issues:

  • Understanding MDR – 8 Important Changes
  • What Is A Medical Device?
  • The MDR & The Authorised Representative
  • The Role of the PRRC Under MDR
  • What Will Happen to UDI’s Under MDR?
  • Clinical Evaluation Report Requirements Under MDR 1
  • Post Market Surveillance Requirements 1
  • Clinical Investigations Under MDR
  • Conformity Assessment Routes Under MDR

Get your copy of the guide by completing your details below, and don’t forget to tick the box to subscribe to our monthly newsletter.