Risk Management in Medical Device | |
Application of any risk management process per the relevant regulations such as FDA or ISO needs to be supported by a risk management framework. Risk Management in Medical Device product development lifecycle is an integrated part. It assures the reliability of the product, performance as expected, and no harm to patients, operators, and the environment. This framework encompasses the procedures of the actual development of the device and the definitions of roles and responsibilities for people associated with the device development project. | |
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Target State: All States Target City : All Cities Last Update : Mar 11, 2025 5:03 AM Number of Views: 91 | Item Owner : Qualysec Contact Email: (None) Contact Phone: (None) |
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