Clinical Evaluation and Labelling: How They Are Interlinked

ShareThoughts2025-01-23T06:22:14+00:00

How Clinical Evaluation and Labelling Work Together Clinical evaluation and labelling form two integral components of the regulatory framework under the European Union Medical Device Regulation (MDR) 2017/745. Though quite distinct, these two processes are intricately related and perform complementary functions for compliance with the requirements imposed by the GSPRs contained in Annex I of the MDR. Multiple guidance documents issued by the Medical Device Coordination Group (MDCG) provide detailed insights into this interdependence: MDCG 2020–13 emphasizes the importance of taking all necessary steps to ensure that medical devices are safe, effective, and compliant with regulatory requirements. MDCG 2021–24 explains how [...]

Successful Clinical Evaluation Report under MDR 2017/745

2025-01-24T06:07:09+00:00

Key Components of a Successful Clinical Evaluation Report under MDR 2017/745 A Clinical Evaluation Report (CER) becomes an essential document in terms of safety and performance of the device to prove that a device is safe and performs as intended. These are the key components of a successful CER within the framework of MDR 2017/745. Scope and Objectives The first and foremost stage in the preparation of the Clinical evaluation report includes and emphasizes the clear definition of its respective scope and objectives. Aspects of this include defining the description of the device, of its intended purpose. This must include risk classification [...]

Clinical Evaluation Report

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