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GLOSSARYEU

Clinical Evaluation

A systematic and planned process of continuously generating, collecting, analyzing, and assessing clinical data on a device. The purpose is to verify the device's safety and performance, including clinical benefits, when used as the manufacturer intends. The results are documented in a clinical evaluation report.

Where it is written
Regulation (EU) 2017/745, Article 2(44); Article 61(12)

Avoid This Mistake

The definition describes a continuing process, not a one-time report.

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