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Database: 365,228(8 Aug 2026)

medical experiment method

medical experiment method, Total:247 items.

The international standard classification for "medical experiment method" includes: Laboratory medicine , Medical Sciences and health care facilities in general , Education , Quality management and quality assurance , Medical microbiology , Transfusion, infusion and injection equipment , Acoustics and acoustic measurements , Implants for surgery, prosthetics and orthotics , Product and company certification. Conformity assessment .

The Chinese standard classification for "medical experiment method" includes: Medical apparatus and devices in general , Medical laboratory equipment , Medical science , Special instruments for teaching , Medical sanitary products , General and microsurgical devices , Underwater sound equipment , Legal medical expert , Sanitation in general , Orthopedic devices , Standardization and Quality Management .


Group Standards of the People's Republic of China

  • T/CAQI 384-2024 Medical laboratories Data item code
  • T/SZAS 10-2019 Medical laboratories management standard
  • T/GDPHA 034-2021 Regulation and implementing measure for grade evaluation of medical research laboratory in Guangdong Province
  • T/NAHIEM 27-2020 Basic Requirements for the Design and Construction of Medical Laboratories
  • T/SZAS 11-2019 Medical laboratories evaluation standard
  • T/CNMIA 0034-2021 Third-party medical testing (immunization) laboratory
  • T/CMBA 023-2024 Requirements for construction and management of biomedical research laboratories
  • T/CBDA 60-2022 Technical specification for decoration of green medical laboratory
  • T/CAME 15-2020 Building technical specifications for medical laboratories

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

  • GB/T 16175-1996 Organic silicon material for medical use-Biological evaluation test methods
  • GB/T 16886.20-2015 Biological evaluation of medical devices―Part 20:Principles and methods for immunotoxicology testing of medical devices
  • GB/T 22576-2008 Medical laboratories - Particular requirements for quality and competence
  • GB/Z 30154-2013 Medical laboratories—Guidance on laboratory implementation of GB/T 22576—2008
  • GB 19781-2005 Medical laboratories—Requirements for safety
  • GB/T 21747-2008 Educational laboratory equipment—Safety requirements and test methods for laboratory workbenches
  • GB/T 14233.2-2005 Test methods for infusion, transfusion, injection equipment for medical use-Part 2: Biological test methods
  • GB/T 16175-2008 Biological evaluation test methods for medical organic silicon materials
  • GB/T 27409-2010 Application of proficiency testing in the medical laboratory
  • GB/T 21919-2008 Laboratory medicine - Requirements for reference measurement laboratories
  • GB/T 31014-2014 Acoustics―Laboratory methods of underwater target strength measurement
  • GB/Z 43280-2023 Medical laboratories—Practical guidance for the estimation of measurement uncertainty
  • GB/T 43278-2023 Medical laboratories—Application of risk management to medical laboratories

未注明发布机构

司法部

  • SF/T 0112-2021 Implemental specification of clinical forensic imaging examination

Shanghai Provincial Standard of the People's Republic of China

Professional Standard - Commodity Inspection

  • SN/T 3955.1-2014 Breeding method of important vectors at frontier ports - Part 1: Breeding method of Anopheles sinensis (An.anthropophagus)
  • SN/T 3955.4-2014 Breeding method of important vectors at frontier ports - Part 4: Breeding method of Musca domestica (Muscina Stabulans)
  • SN/T 3955.5-2014 Breeding method of important vectors at frontier ports - Part 5:Breeding method of Blattella germanica (Periplaneta americana,Periplaneta australasiae,Periplaneta brunnea)
  • SN/T 3955.2-2014 Breeding method of important vectors at frontier ports - Part 2:Breeding method of Aedes albopicuts (Aedes aegypti)
  • SN/T 3955.6-2014 Breeding method of important vectors at frontier ports - Part 6: Breeding method of Xenopsylla cheopis (Pulex irritans, Citellophilus tesquorum)

Professional Standard - Medicine

Guizhou Provincial Standard of the People's Republic of China

  • DB52/T 1565-2021 Acceptance specification for medical laboratory ventilation system

国家质量监督检验检疫总局

  • SN/T 3955.3-2014 Breeding method of important vectors at frontier ports - Part 3: Breeding method of Culex pipiens pallens (Cx.pipiens quinque fasciatus)

Professional Standard - Hygiene

  • WS/T 418-2024 Guide to Selecting a Medical Laboratory
  • WS/T 255-2005 Clinical laboratory medicine-Requirements for reference measurement laboratories

Beijing Provincial Standard of the People's Republic of China

Professional Standard - Public Safety Standards

Shanxi Provincial Standard of the People's Republic of China

  • DB14/T 2797-2023 Specifications for confirmation of chemical analysis methods in testing laboratories
  • DB14/T 2798-2023 Specification for verification of chemical analysis methods in testing laboratories

国家市场监督管理总局、中国国家标准化管理委员会

  • GB/T 22576.7-2021 Medical laboratories—Requirements for quality and competence—Part 7:Requirements in the field of transfusion medicine

国家药监局

  • YY/T 1832-2022 Implants for sports medicine-Tensile testing method for suture

国家市场监督管理总局

  • RB/T 060.2-2021 Forensic Identification/Forensic Science Proficiency Testing Implementation Guide Part 2: Forensic Clinical Identification
  • RB/T 060.1-2021 Guidance on the implementation of proficiency testing in forensic science—Part 1:Forensic pathology examination
  • RB/T 060.3-2021 Forensic Identification/Forensic Science Proficiency Testing Implementation Guide Part 3: Forensic Toxicology Identification

SCC

Korean Agency for Technology and Standards (KATS)

  • KS P ISO 22367-2023 Medical laboratories — Application of risk management to medical laboratories
  • KS P ISO 15190:2021 Medical laboratories — Requirement for safety
  • KS P ISO 15190-2010(2016) Medical laboratories-Requirements for safety
  • KS P ISO 15195-2014(2019) Laboratory medicine — Requirements for reference measurement laboratories
  • KS P ISO TR 22869-2009(2019) Medical laboratories-Guidance on laboratory implementation of KS P ISO 15189:2006
  • KS P ISO 15190:2010 Medical laboratories-Requirements for safety
  • KS P ISO 15195:2007 Laboratory medicine-Requirements for reference measurement laboratories
  • KS P ISO TR 22869-2019 Medical laboratories-Guidance on laboratory implementation of KS P ISO 15189:2006
  • KS P ISO 15195:2014 Laboratory medicine — Requirements for reference measurement laboratories
  • KS P ISO TR 22869:2009 Medical laboratories-Guidance on laboratory implementation of KS P ISO 15189:2006
  • KS P ISO 15195-2019 Laboratory medicine — Requirements for reference measurement laboratories
  • KS P ISO 15189-2019 Medical laboratories ─ Requirements for quality and competence
  • KS P ISO 15189-2013(2019) Medical laboratories ─ Requirements for quality and competence
  • KS P 2068-2020 Protocol for interference testing in in-vitro diagnostic medical laboratory
  • KS P 1977-2023 Protocol for evaluation of qualitative test performance in in-vitro diagnostic medical laboratory
  • KS P 1975-2018 Protocol for evaluation of precision performance of the quantitative test in in-vitro diagnostic medical laboratory
  • KS P 1975-2023 Protocol for evaluation of precision performance of the quantitative test in in-vitro diagnostic medical laboratory
  • KS P 2069-2020 Protocol for evaluation of detection capability for measurement procedures in in-vitro diagnostic medical laboratory
  • KS P ISO 15189:2011 Medical laboratories-Particular requirements for quality and competence
  • KS P ISO 15189:2013 Medical laboratories ─ Requirements for quality and competence
  • KS P ISO 10993-20-2009(2019) Biological evaluation of medical devices-Part 20:Principles and methods for immunotoxicology testing of medical devices
  • KS P ISO 10993-20-2019 Biological evaluation of medical devices-Part 20:Principles and methods for immunotoxicology testing of medical devices

ES-UNE

  • UNE-EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
  • UNE-ISO 15190:2022 Medical laboratories — Requirements for safety
  • UNE-EN ISO 15189:2023 Medical laboratories - Requirements for quality and competence (ISO 15189:2022)
  • UNE-EN ISO 15195:2019 Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018)

Standard Association of Australia (SAA)

German Institute for Standardization

  • DIN EN ISO 22367:2020-09 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020); German version EN ISO 22367:2020
  • DIN 58956-3:1986-12 Medical microbiology; medical microbiological laboratories; requirements for the organization scheme
  • DIN EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
  • DIN EN ISO 15195:2004 Laboratory medicine - Requirements for reference measurement laboratories (ISO 15195:2003); German version EN ISO 15195:2003
  • DIN 58956-10:1986-01 Medical microbiology; medical-microbiological laboratories; safety marking
  • DIN 58956-5:1990 Medical microbiology; medical-microbiological laboratories; hygiene scheme requirements
  • DIN 58956-2:1986-01 Medical microbiology; medical microbiological laboratories; requirements for equipment
  • DIN 58985:2003 Laboratory medicine - Decision-marking criteria
  • DIN EN ISO 8325:2004 Dentistry - Test methods for rotary instruments (ISO 8325:2004); German version EN ISO 8325:2004
  • DIN EN ISO 15189:2023-03 Medical laboratories - Requirements for quality and competence (ISO 15189:2022); German version EN ISO 15189:2022
  • DIN 58956-2:1986 Medical microbiology; medical microbiological laboratories; requirements for equipment
  • DIN 58956-10:1986 Medical microbiology; medical-microbiological laboratories; safety marking
  • DIN EN ISO 15195:2019-07 Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018); German version EN ISO 15195:2019
  • DIN 58956-4:1986 Medical microbiology; medical-microbiological laboratories; waste disposal; safety requirements and testing
  • DIN EN ISO 15189:2007 Medical laboratories - Particular requirements for quality and competence (ISO 15189:2007); English version of DIN EN ISO 15189:2007-08
  • DIN EN ISO 15189:2023 Medical laboratories - Requirements for quality and competence (ISO 15189:2022)
  • DIN EN 1614:2006-12 Health informatics - Representation of dedicated kinds of property in laboratory medicine; English version EN 1614:2006
  • DIN 58956-3:1986 Medical microbiology; medical microbiological laboratories; requirements for the organization scheme

Association Francaise de Normalisation

International Organization for Standardization (ISO)

  • ISO 22367:2020 Medical laboratories — Application of risk management to medical laboratories
  • ISO 15190:2003 Medical laboratories - Requirements for safety
  • ISO 15190:2020 Medical laboratories — Requirements for safety
  • ISO 15195:2003 Laboratory medicine - Requirements for reference measurement laboratories
  • ISO/TR 22869:2005 Medical laboratories - Guidance on laboratory implementation of ISO 15189:2003
  • ISO 15189:2012 Medical laboratories - Requirements for quality and competence
  • ISO 15189:2003 Medical laboratories - Particular requirements for quality and competence
  • ISO 15189:2007 Medical laboratories - Particular requirements for quality and competence
  • ISO 15189:2022 Medical laboratories — Particular requirements for quality and competence
  • ISO/DTS 23824:2024 Medical laboratories - Guidance on application of ISO 15189 in anatomic pathology
  • ISO 15195:2018 Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures
  • ISO 16140-4:2020/CD Amd 2 Microbiology of the food chain-Method validation-Part 4: Protocol for method validation in a single laboratory
  • ISO/DIS 5649:2024 Medical laboratories — Concepts and specifications for the design, development, implementation, and use of laboratory-developed tests
  • ISO 16140-4:2020 Microbiology of the food chain — Method validation — Part 4: Protocol for method validation in a single laboratory

GOST

British Standards Institution (BSI)

RU-GOST R

  • GOST 28311-1989 Laboratory medical dosers. General technical requirements and test methods
  • GOST 28311-2021 Medical laboratory dosers. General technical requirements and test methods
  • GOST R ISO 15195-2006 Laboratory medicine. Requirements for reference measurement laboratories
  • GOST R 52960-2008 Forensic science laboratories accreditation. Guidance on the application of GOST R ISO/IEC 17025
  • GOST R 53133.2-2008 Medical laboratory technologies. Quality control of clinical laboratory tests. Part 2. Rules for intra-laboratory quality control of quantitative methods of clinical laboratory tests using control materials
  • GOST R 53079.1-2008 Medical laboratory technologies. Quality assurance of clinical laboratory tests. Part 1. Rules for description of methods of clinical laboratory tests
  • GOST R 51758-2001 Nutrient media for veterinary purposes. Methods of biological testing
  • GOST R ISO 15189-2006 Medical laboratories. Particular requirements for quality and competence
  • GOST R ISO 15189-2015 Medical laboratories. Particular requirements for quality and competence
  • GOST R 52770-2016 Medical devices. Safety requirements. Methods of sanitation-chemical and toxicological tests
  • GOST R 52770-2007 Medical products. Safety requirements. Methods of sanitation-chemical and toxicological tests

European Committee for Standardization (CEN)

  • EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
  • EN ISO 15195:2003 Laboratory medicine - Requirements for reference measurement laboratories (ISO 15195:2003)
  • EN ISO 15189:2022/A11:2023 Medical laboratories - Requirements for quality and competence
  • EN ISO 15189:2012 Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)
  • EN ISO 15189:2003 Medical laboratories - Particular requirements for quality and competence ISO 15189: 2003
  • EN ISO 15189:2022 Medical laboratories - Requirements for quality and competence (ISO 15189:2022)
  • prEN ISO 15189:2021 Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2021)
  • EN 1614:2006 Health informatics - Representation of dedicated kinds of property in laboratory medicine

GOSTR

  • GOST R ISO/TR 22869-2009 Medical laboratories. Quidance on laboratory implementation of ISO 15189:2003
  • GOST R 52905-2007 Mеdical laboratories. Requirements for safety
  • GOST R 52770-2020 Medical devices. Evaluation system of biological effects. Part 1. General requirements for biological safety

GSO

Military Standards (MIL-STD)

CEN - European Committee for Standardization

  • EN ISO 15195:2019 Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures
  • DD ENV 1613-1995 Medical Informatics - Messages for exchange of laboratory information
  • EN ISO 15189:2007 Medical laboratories - Particular requirements for quality and competence

TH-TISI

  • TIS 2276-2006 Medical laboratories.requirements for safety
  • TIS 2277-2006 Laboratory medicine.requirements for reference measurement laboratories
  • TIS 2154-2004 Medical laboratories.particular requirements for quality and competence

KR-KS

  • KS P ISO 15190-2021 Medical laboratories — Requirement for safety
  • KS P 1977-2018(2023) Protocol for evaluation of qualitative test performance in in-vitro diagnostic medical laboratory
  • KS P 1975-2018(2023) Protocol for evaluation of precision performance of the quantitative test in in-vitro diagnostic medical laboratory
  • KS Q ISO 15189-2024 Medical laboratories — Requirements for quality and competence
  • KS P ISO TS 20914-2022 Medical laboratories — Practical guidance for the estimation of measurement uncertainty

US-CLSI

AENOR

  • UNE-ISO/TR 22869:2007 IN Medical laboratories. Guidance on laboratory implementation of ISO 15189: 2003. (ISO/TR 22869:2005)
  • UNE-EN ISO 15195:2004 Laboratory medicine - Requirements for reference measurement laboratories (ISO 15195:2003)

Canadian Standards Association (CSA)

  • CSA ISO 22367:2021 Medical laboratories - Application of risk management to medical laboratories (Adopted ISO 22367:2020, first edition, 2020-02)
  • CAN/CSA-Z15190-2005 Medical laboratories - Requirements for safety (First Edition)

Indonesia Standards

Danish Standards Foundation

American Society for Testing and Materials (ASTM)

  • ASTM E2763-10 Standard Practice for Computer Forensics
  • ASTM E1492-11(2017) Standard Practice for Receiving, Documenting, Storing, and Retrieving Evidence in a Forensic Science Laboratory
  • ASTM E1492-92(1999) Standard Practice for Receiving, Documenting, Storing, and Retrieving Evidence in a Forensic Science Laboratory

Institute of Electrical and Electronics Engineers (IEEE)

Lithuanian Standards Office

  • LST EN ISO 15195:2004 Laboratory medicine - Requirements for reference measurement laboratories (ISO 15195:2003)
  • LST EN ISO 15189:2013 Medical laboratories - Requirements for quality and competence (ISO 15189:2012)

NZ-SNZ

  • NZS/ISO 15189:2007 Medical Laboratories - Particular Requirements for Quality and Competence

ZA-SANS

  • SANS 15189:2009 Medical laboratories - Particular requirements for quality and competence

VN-TCVN

  • TCVN 7782-2008 Medical laboratories.Particular requirements for quality and competence

TR-TSE