Clinical Evaluation Plan and Report (CEP, CER) White Paper

Cormica’s white paper, written by Uday Kuppam, Clinical Evaluation Specialist at MET, offers essential guidance for medical device manufacturers navigating the evolving regulatory landscape for Class I devices under EU MDR 2017/745 and UK MDR 2002. Covering CE and UKCA marking, technical documentation, clinical evaluation (CEP/CER), and post-market obligations, this resource is designed to support compliance and accelerate market entry.

Read the white paper on Cormica's website here