Discover the key steps for launching Class I medical devices in the UK and EU. From CE/UKCA marking to clinical evaluation and documentation, this Cormica white paper is a must-read for manufacturers. Read here
News
Date of event 2nd April 2025
Read Cormica's White Paper on Clinical Evaluations and Reports (CEP, CER) for launching Class I Medical Devices in the UK/EU.
Discover the key steps for launching Class I medical devices in the UK and EU. From CE/UKCA marking to clinical evaluation and documentation, this Cormica white paper is a must-read for manufacturers. Read here