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ISO 14971 Risk Management in Medical Devices

31.05.2024
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ISO 14971 Risk Management in Medical Devices

Risk Management in Medical Devices This standard encompasses a process for manufacturers to identify the hazards associated with medical devices, including in vitro diagnostic (IVD) devices, estimate and evaluate the associated risks, control these risks, and monitor the effectiveness of these controls. Training ISO 14971 risk management training, under the Medical Device Regulation (MDR), is essential for all medical device manufacturers. By the end of this training, participants will have the necessary tools to manage product risks in compliance with an international standard.

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