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Database: 365,228(8 Aug 2026)

clinical diagnosis laboratory diagnosis

clinical diagnosis laboratory diagnosis, Total:74 items.

The international standard classification for "clinical diagnosis laboratory diagnosis" includes: Medical Sciences and health care facilities in general , Veterinary medicine , Laboratory medicine .

The Chinese standard classification for "clinical diagnosis laboratory diagnosis" includes: Sanitation in general , Animal quarantine, veterinary and epidemic prevention , Medical laboratory equipment , Diagnostic standard for public nuisance diseases .


Professional Standard - Hygiene

  • WS/T 489-2016 Laboratory diagnosis of urinary tract infections
  • WS/T 489-2015 Clinical Microbiological Laboratory Diagnosis of Urinary Tract Infection

中华人民共和国国家卫生和计划生育委员会

  • WS/T 208-2001 Clinical diagnostic standard for dental fluorosis
  • WS/T 497-2017 Performance guideline for clinical laboratory diagnosis of invasive fungal diseases
  • WS/T 124-1999 Inspection criteria of the quality of clinical chemistry in vitro diagnostic kits - General guideline
  • WS/T 498-2017 Performance guideline for clinical laboratory diagnosis of bacterial diarrhea

Fujian Provincial Standard of the People's Republic of China

Hebei Provincial Standard of the People's Republic of China

  • DB13/T 5374-2021 Technical rules for comprehensive diagnosis of poultry aspergillosis fumigatus
  • DB13/T 5584-2022 Technical regulations for diagnosis, prevention and treatment of Trichophyton palpebrata
  • DB13/T 2892-2018 Technical regulations for comprehensive diagnosis of avian candidiasis
  • DB13/T 5573-2022 Technical regulations for comprehensive diagnosis of chicken fecal enterococci

Professional Standard - Agriculture

Xizang Provincial Standard of the People's Republic of China

  • DB54/T 0159-2018 Method for hatching and diagnosing the miracidium of oriental flukes in cattle and sheep

国家市场监督管理总局、中国国家标准化管理委员会

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

Jiangxi Provincial Standard of the People's Republic of China

  • DB36/T 1747-2023 Diagnostic technical rules for novel goose astrovirus disease
  • DB36/T 1622-2022 Technical specifications for clinical diagnosis of aquatic animal diseases

农业农村部

Jilin Provincial Standard of the People's Republic of China

  • DB22/T 3473-2023 Etiological diagnosis technology of bovine respiratory syncytial disease

Group Standards of the People's Republic of China

  • T/SHZSAQS 0164-2022 Technical rules for diagnosis of bovine viral diarrhea and mucous membrane disease
  • T/CADERM 9101-2023 Diagnostic requirements for magnetocardiogram of myocardial ischemia in clinical application

Hubei Provincial Standard of the People's Republic of China

Professional Standard - Medicine

  • YY/T 1227-2014 In vitro diagnostic reagent(kit)nomenclature for clinical chemistry

Jiangsu Provincial Standard of the People's Republic of China

Shandong Provincial Standard of the People's Republic of China

RU-GOST R

  • GOST R 51352-1999 Kits of reagents for clinical laboratory diagnostics. Test methods
  • GOST R 51088-1997 Kits of reagents for clinical laboratory diagnostics. General specifications
  • GOST R 57003-2016 Diagnostics in oncology. Diagnostic algorithms. Solid intrathoracic tumors. Laboratory stage
  • GOST R 57004-2016 Diagnostics in oncology. Diagnostic algorithm. Cervix. Laboratory stage
  • GOST R 53079.2-2008 Medical laboratory technologies. Quality assurance of clinical laboratory tests. Part 2. Guidelines for improvements of quality in clinical-diagnostic laboratory. Typical model
  • GOST R 55457-2013 Horses. Methods for laboratory helminthosis diagnostics
  • GOST 26075-2013 Animals. Methods of Laboratory Diagnostic of Rabies
  • GOST R 53133.1-2008 Clinical laboratory technologies. Quality control of clinical laboratory tests. Part 1. Limits of allowable errors of the results of the analyte measurements in clinical-diagnostics laboratories

HU-MSZT

Korean Agency for Technology and Standards (KATS)

  • KS P ISO TR 18112:2009 Clinical laboratory testing and in vitro diagnostic test systems-In vitro diagnostic medical devices for professional use-Summary of regulatory requirements for information supplied by the manufacturer
  • KS P ISO TR 18112-2009(2014) Clinical laboratory testing and in vitro diagnostic test systems-In vitro diagnostic medical devices for professional use-Summary of regulatory requirements for information supplied by the manufacture
  • KS P ISO TR 18112-2020 Clinical laboratory testing and in vitro diagnostic test systems-In vitro diagnostic medical devices for professional use-Summary of regulatory requirements for information supplied by the manufacturer
  • KS P ISO 19001:2010 In virto diagnostic medical devices-Information supplied by the manufacturer with in vitro gnostic reagents for staining in biology
  • KS P ISO 15198:2006 Clinical laboratory medicine-In vitro diagnostic medical devices-Validation of user quality control procedures by the manufacturer
  • KS P ISO 15198:2017 Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer

German Institute for Standardization

  • DIN 6809-3:1990 Clinical dosimetry; diagnostic radiology
  • DIN 58937-7:1994 General laboratory medicine (clinical pathology); part 7: listing of features of in vitro diagnostic systems

International Organization for Standardization (ISO)

  • ISO/TR 18112:2006 Clinical laboratory testing and in vitro diagnostic test systems - In vitro diagnostic medical devices for professional use - Summary of regulatory requirements for information supplied by the manufacturer
  • ISO 19001:2002 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • ISO 19001:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • ISO 15198:2004 Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer

European Committee for Standardization (CEN)

  • EN ISO 19001:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology

Indonesia Standards

  • SNI ISO 19001:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology

KR-KS

  • KS P ISO 15198-2017 Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer
  • KS P 2170-2022 Protocol for analytical performance evaluation of infectious disease molecular diagnosis in in-vitro diagnostic medical laboratory

SCC

  • 06/30146522 DC BS ISO 18113-4. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 4. In vitro diagnostic reagents for self-testing
  • 06/30146518 DC BS ISO 18113-3. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 3. In vitro diagnostic instruments for professional use
  • 06/30146526 DC BS ISO 18113-5. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 5. In vitro diagnostic instruments for self-testing
  • 06/30146515 DC BS ISO 18113-2. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 2. In vitro diagnostic reagents for professional use