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发表于 2024-5-15 13:50:10
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摘自BSI 对于MDR的文件清单guidance,可以都了解一下
2.1.6 Instructions for use /Device Operating Manual(s)
Manufacturers must ensure that the information within the IFUs, especially related to intended purpose, indications, contra-indications, and other safety related information such as side effects, warnings is aligned with similar information from other sections such as risk management, clinical evaluation etc. IFUs must contain all the information required as per applicable requirements specified within GSPR 23. Manufacturers must as a minimum submit the English version at the time of application.
2.1.7 Patient handbook Some devices incorporate all the information relevant for the patient/user within the IFU itself. Some devices are accompanied by a patient handbook with additional instructions specific to the patient, for example with devices (or parts, components of the devices) that are patient operated. If the device is supplied with a patient handbook, this should be provided.
2.1.8 Physicians handbook If a separate physicians’ handbook is relevant for the device, this should be provided. |
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