Clinical Evaluation Report

A documented analysis of clinical data proving a device's safety, performance, and risk-benefit ratio.

A Clinical Evaluation Report (CER) is a requirement under European regulatory frameworks such as the MDR. It synthesizes literature reviews, clinical investigations, and post-market data to demonstrate that the device achieves its intended clinical purpose without posing unacceptable risks.

Explore the data behind the terms

HaRi brings the FDA, MHRA, EUDAMED, Health Canada and TGA registers into one search: devices, manufacturers, product codes and safety events, all cross-referenced and free to explore.