Clinical Evaluation Report
If manufacturers want to place your devices in European Market, they must prepare and maintain a clinical evaluation report that complies with the requirements of MEDDEV 2.7.1. rev. 4 and EU MDR Article 61 and Annex XIV part A.
https://mavenprofserv.com/clinical-evaluation-report/
https://mavenprofserv.com/clinical-evaluation-report/
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