Guidelines for clinical evaluation using real world data

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In: Medicine/medical devices, specifications
The National medical product administration released the technical guidelines for clinical evaluation of medical devices with real world data on November 24. Real world data include, but are not limited to: Generated in the process of providing and paying for health care services, it is generated based on management purposes, such as hospital electronic medical record data, medical insurance data, health records, etc.Based on the research purpose of establishing the database, a unified data standard and data collection mode should be established, and the data resources formed and established in routine clinical practice, such as device registration data, etc. RealRead More →

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