GB/T 22576.1-2018Medical laboratories - Requirements for quality and competence - Part 1: General requirements (English PDF)
医学实验室 质量和能力的要求 第1部分：通用要求
GB/T 22576.1 | Evolution and historical versions
| Std ID | Title | Status |
|---|---|---|
| GB/T 22576.1-2026 | Medical laboratories - Requirements for quality and competence - Part 1: General requirements | Valid |
| GB/T 22576.1-2018 | Medical laboratories - Requirements for quality and competence - Part 1: General requirements | Obsolete |
GB/T 22576.1-2018 is obsolete. It has been replaced by GB/T 22576.1-2026. This page sells the obsolete edition, for projects and contracts that still cite it.
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Issued by
State Administration for Market Regulation; Standardization Administration of China
Level / Type
National · Recommended
Issue date
December 28, 2018
Implementation date
July 1, 2019
Scope
GB/T 22576.1-2018 is the English-translated version of 医学实验室 质量和能力的要求 第1部分：通用要求.
GB/T 22576.1-2018 is the Chinese national standard "Medical laboratories - Requirements for quality and competence - Part 1: General requirements". It was issued on December 28, 2018 by the State Administration for Market Regulation and the Standardization Administration of China, and took effect on July 1, 2019. It is obsolete: it has been replaced by GB/T 22576.1-2026.
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Document preview — GB/T 22576.1-2018
National Standard of the People's Republic of China
Issued by: State Administration for Market Regulation; Standardization Administration of China
Contents
- Document data
1 Document data
Sector: National standard (Recommended).
Issuing body: State Administration for Market Regulation; Standardization Administration of China.
Date of issue: 2018-12-28.
Date of implementation: 2019-07-01.
Status: obsolete, replaced by GB/T 22576.1-2026.
......
This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — all pages — is available in the English PDF.
Referenced standards
Cited by
- GB/Z 136-2026Medical laboratories - Reagents for staining biological specimen - Guidance for users
- GB/T 39367-2025In vitro diagnostic test systems - Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens - Laboratory quality practice guide
- GB/T 42080.3-2024DNA Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA
- GB/T 42216.4-2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: In situ detection technique
- GB/T 44467-2024Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA
- GB/T 44586.1-2024In vitro diagnostic medical devices - Multiplex molecular testing for nucleic acids - Part 1: Terminology and general requirements for nucleic acid quality evaluation
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Related Standards
GB/T 22576.2-2021 — Medical laboratories - Requirements for quality and competence - Part 2: Requirements in the field of clinical hematological examination
GB/T 22576.3-2021 — Medical laboratories—Requirements for quality and competence—Part 3: Requirements in the field of urine examination
GB/T 22576.4-2021 — Medical laboratories—Requirements for quality and competence—Part 4: Requirements in the field of clinical chemistry examination
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GB/T 22576.1-2018
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