Medical Device Clinical Strategy & Requirements Workshop
Hempsons 100 Wood Street, London, United KingdomClinical strategy, evidence and evaluation are central to product approval and market access. It’s a requirement of the new EU Medical Device Regulation (MDR: article 61) that a medical device company have a regulatory strategy and of the MDR and MEDDEV 2.7/1 rev 4 that the company have a clinical evaluation strategy. In order to […]