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WS/T 230-2024 PDF English

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WS/T 230-2024: Guidelines for implementation of real-time fluorescent polymerase chain reaction in clinical laboratories.
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WS/T 230: Historical versions

Std IDVersionUSDBuyDeliver [PDF] inTitle (Description)
WS/T 230-2024English529 Add to Cart 4 days [Need to translate] Guidelines for implementation of real-time fluorescent polymerase chain reaction in clinical laboratories.
WS/T 230-2002English559 Add to Cart 3 days [Need to translate] Guidelines for use of polymerase chain reaction (PCR) technique in clinical diagnosis

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Basic data

Standard ID WS/T 230-2024 (WS/T230-2024)
Description (Translated English) Guidelines for implementation of real-time fluorescent polymerase chain reaction in clinical laboratories.
Sector / Industry Health Industry Standard (Recommended)
Classification of Chinese Standard C50
Classification of International Standard 11.020
Word Count Estimation 24,218
Date of Issue 2024-05-09
Date of Implementation 2024-11-01
Older Standard (superseded by this standard) WS/T 230-2002
Issuing agency(ies) National Health Commission
Summary This standard specifies the requirements for sample collection and processing, methods, pollution prevention and control, quality management, result interpretation and reporting, laboratory biosafety, and clinical scope of application of real-time fluorescent polymerase chain reaction in clinical laboratory applications. This standard applies to qualitative and quantitative detection of nucleic acid amplification genes by medical and health institutions and medical testing laboratories at all levels and types across the country. This standard does not apply to detection based on technologies such as nucleic acid hybridization, nucleic acid isothermal amplification, and gene sequencing.

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