Single Plasma Station Technical Operation Regulations Renewal National Health and Health Commission: User face recognition and verification of blood donor identity

Cover news reporter Shao Meng

On July 20, the cover journalist learned from the National Health and Health Commission that in order to further improve the standardized practice level of single -mining plasma stations, improve the quality of plasma, and ensure the safety of blood donors, the National Health and Health Commission recently issued the "Single Plasma Station Technology Operation Regulations (2022) (2022) "(referred to as" Regulations "), it is required to strengthen the management of plasma stations alone, and use face recognition technology to verify the identity of blood donors.

Data map. Xinhua News Agency reporter Cao Zhengping by Cao Zhengping (has nothing to do with graphic)

According to reports, the former Ministry of Health formulated and released the "Single Plasma Station Technical Operation Regulations" in 2011. The new "Regulations" was revised and improved on the basis of this. It will be implemented from October 1, 2022. "Single Plasma Station Technical Operation Regulations" was abolished at the same time.

The reporter noticed that the revised "Regulations" total 5 chapters and 9 appendix. First of all, the management of blood donors is strengthened. The "Regulations" clearly requires the use of face recognition technology to verify the identity of the vendor, and compare the on -site photos of the plasma with their ID card. The comparison value of recognition similarity is registered after consistent. At the same time, the content of the content before refining the plasma is refined, and the classification management requirements for the classification of blood donors are proposed.

Secondly, further refine the requirements for slurry personnel, collect materials and equipment, and add samples and management requirements for specimens. The "Regulations" mentioned that according to the detection process of test items, blood product production units and the needs of nucleic acid testing, specific sample standards are formulated. In accordance with the technical requirements of each test, the proper specimen can be used to retain the specimen to ensure that the specimen volume is sufficient during the test.

In addition, the detection methods and standards of blood testing projects were adjusted, the testing equipment and management requirements were updated, the plasma detection process was further refined, and the centralized testing requirements of the solo plasma station were added. Adjust the laboratory environment and facilities, personnel qualifications, personnel protection, instruments and equipment, reagents and consumables in the laboratory environment and facilities, personnel qualifications, personnel protection, instruments and equipment, reagents and consumables.

The "Regulations" further refine the content of the plasma outbound review, clarify the processing process of unqualified plasma, and strengthen the management of non -qualified plasma. It is mentioned that plasma status is divided into qualification, to be tested and unqualified. Establish a qualified product area, to be tested and unqualified, and there are obvious signs. The plasma classification of different states is stored in the corresponding storage area. Unqualified plasma should be physically isolated to prevent misunderstanding of unqualified plasma.

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