Are you ready for the new EU MEDDEV regulations?
Establishing state of the art for a medical device is a critical component of a MEDDEV 2.1/7 rev 4 compliant Clinical Evaluation Report (CER). In partnership with Criterion Edge, we have developed a white paper on establishing state of the art. Through this white paper you will:
- Gain an understanding of the meaning of "state of the art" as it pertains to MEDDEV 2.7/1 rev 4
- Learn how to establish sound methods to identify and select pertinent literature
- Find out how to efficiently produce and maintain fully compliant and audit ready state of the art descriptions using DistillerSR
Download your copy now!