Refine by
Clinical Data Evaluation Equipment & Supplies
1 equipment items found
by:Sterling Medical Devices based inMoonachie, NEW YORK (USA)
All medical devices sold in the EU must have a Clinical Evaluation Report (CER) as part of its technical documentation to satisfy the new EU Medical Device Regulation (MDR) requirements. A comprehensive analysis of pre- and post-market data relevant to a medical device, a Clinical Evaluation Report demonstrates ...