How the EU MDR Impacts Medical Writing

11:55 AM - 12:30 PM

With heightened requirements on clinical evaluation and clinical data under the European Union Medical Device Regulation (MDR), many medical device manufacturers are forced to rethink their clinical strategy. Companies that haven’t conducted any clinical investigations are suddenly facing new challenges such as planning studies and completing clinical evaluations based on their own data. As a result, clinical operations and medical writing have become an essential asset to many MedTech companies. In this session, the speaker will highlight how skills and experience in medical writing can help bring value to MedTech companies in the new MDR/IVDR era.