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The National Medical Products Administration has issued the "In vitro diagnostic test systems - Performance evaluation method - Part 5: Analytical specificity", which was implemented on May 1, 2024.
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Publish time：2024-05-27
转自：
中华人民共和国
医
药行业标准
YY/T 1789.5-2023
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Legend Biotechnology at the Eighth Medical Industry Meeting of Yunnan Province
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The Issuance and Implementation of the Classification Rules for In Vitro Diagnostic Reagents
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