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Phase I Clinical Phase II Clinical

Phase I Clinical Phase II Clinical, Total:170 items.

The international standard classification for "Phase I Clinical Phase II Clinical" includes: Medical Sciences and health care facilities in general .

The Chinese standard classification for "Phase I Clinical Phase II Clinical" includes: Medical science , Nutrition sanitation , Sanitation in general , Legal medical expert , Medical apparatus and devices in general .


Group Standards of the People's Republic of China

  • T/CGCPU 025-2022 Guideline of contract research organization
  • T/CACM 1260-2019 Clinical guidelines for diagnosis and treatment of gynecology in TCM Premenstrual syndrome
  • T/CACM 1239-2019 Clinical guidelines for diagnosis and treatment of gynecology in TCM Advanced Menstruation
  • T/DALN 024-2022 Judgment of primary subclinical ketosis in postpartum dairy and meat cattle
  • T/CACM 1300-2019 Clinical guidelines for diagnosis and treatment of gynecology in TCM Ovulation Bleeding
  • T/CACM 1309-2019 Clinical guidelines for diagnosis and treatment of gynecology in TCM Irregular Menstrual Cycle
  • T/CAPA 12-2024 Clinical treatment and long-term management of melasma
  • T/CACM 1126-2018 Traditional Chinese medicine guidelines for the diagnosis and treatment of mental diseases- Premenstrual mental disorder
  • T/SHPPA 023-2023 Long term follow-up study guidance for CAR-T cell therapy products
  • T/CACM 1265-2019 TCM Gynecology Clinical Diagnosis and Treatment Guidelines for Prolonged Menstrual Period
  • T/GDACM 0125-2024 Traditional Chinese medicine external therapy guidelines for adverse reactions of early-stage breast cancer (Ru Yan disease)
  • T/CGCPU 014-2020 The practices of chemicals for clinical trials in clinical trial institutions
  • T/CGCPU 006-2019 Phase I Clinical Trial Capacity Evaluation Criteria
  • T/HNMA 1-2019 MRI clinical function evaluation specification
  • T/CGCPU 025-2023 Guideline of contract research organization
  • T/GDACM 0107-2022 Guidelines for Clinical Diagnosis and Treatment of Early Breast Cancer (Ruyan) with Integrated Traditional Chinese and Western Medicine
  • T/HNMA 3-2019 MRI Clinical Functional Evaluation Guidelines
  • T/CGCPU 006-2023 Specification for competency assessment of phase I clinical trials
  • T/CATCM 033-2025 Standards for the Clinical Application of Traditional Chinese Medicine Preparations
  • T/CACM 1127-2018 Traditional Chinese medicine guidelines for the diagnosis and treatment of mental diseases- Perimenopausal mental disorder
  • T/CACM 1063~1064-2018 Acupuncture Medicine Clinical Basic Terminology Acupuncture Medicine Clinical General Requirements
  • T/CACM 1124~1142-2018 Guidelines for clinical diagnosis and treatment of mental illness in traditional Chinese medicine (II)
  • T/SHZSAQS 00078-2022 Judgment of primary subclinical ketosis in postpartum dairy and meat cattle

Inner Mongolia Provincial Standard of the People's Republic of China

  • DB15/T 1899-2020 Judgment of primary subclinical ketosis in postpartum dairy cows

Anhui Provincial Standard of the People's Republic of China

  • DB34/T 4619-2023 Guidelines for the Construction of Intelligent Research Laboratory for Drug Phase I Clinical Trials

Professional Standard - Agriculture

Professional Standard - Hygiene

Zhejiang Provincial Standard of the People's Republic of China

Professional Standard - Judicatory

Professional Standard - Certification and Accreditation

Professional Standard - Medicine

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

Professional Standard - Public Safety Standards

Ente Nazionale Italiano di Unificazione

US Federal Contractor Registration (USFCR)

Czech Standards Institute (UNMZ)

Kingdom of Bahrain Testing and Metrology Directorate

  • BH GSO ASTM F3108:2023 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Knee Reconstructive Surgery

Clinical and Laboratory Standards Institute

  • CLSI GP46-R-2003 Report on the Challenges of Planning Clinical Laboratory Operations During Disasters
  • CLSI C49-2018 Analysis of Body Fluids in Clinical Chemistry
  • CLSI GP05-A3-2011 Clinical Laboratory Waste Management; Approved Guideline—Third Edition

GCC Standardization Organization

  • GSO ASTM F3108:2022 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Knee Reconstructive Surgery
  • GSO ISO 14155:2015 Clinical investigation of medical devices for human subjects -- Good clinical practice

Canadian General Standards Board (CGSB)

American Society for Testing and Materials (ASTM)

  • ASTM F3108-19 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Knee Reconstructive Surgery
  • ASTM F3448-20 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Hip Reconstructive Surgery

The Directorate General of Specifications and Metrology (DGSM)

  • OS GSO ISO 14155:2015 Clinical investigation of medical devices for human subjects -- Good clinical practice

British Standards Institution (BSI)

  • BS EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects-Clinical investigation plans
  • 08/30116059 DC BS ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
  • 24/30467406 DC BS EN ISO 14155 Clinical investigation of medical devices for human subjects - Good clinical practice
  • BS EN ISO 14155:2020+A11:2024 Clinical investigation of medical devices for human subjects. Good clinical practice
  • 24/30506234 DC BS EN ISO 12487 Medical electrical equipment — Clinical performance evaluation of clinical thermometers
  • BS 691:1966 Clinical maximum thermometers
  • BS 691:1936 Clinical maximum thermometers
  • BS 691:1953 Clinical maximum thermometers
  • 18/30344902 DC BS EN ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
  • BS 691:1961 Clinical maximum thermometers
  • BS EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Clinical investigation plans
  • BS EN ISO 14155:2020 Clinical investigation of medical devices for human subjects. Good clinical practice

Bureau of Indian Standards

  • IS/ISO 14155-2011 Clinical Investigation of Medical Devices for Human Subjects-Good Clinical Practice

Spanish Association for Standardization (UNE)

  • UNE-EN ISO 14155:2021 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • AENOR UNE-EN ISO 14155:2012 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
  • UNE-EN ISO 14155-2:2004 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003)
  • UNE-EN ISO 14155:2012 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)

International Organization for Standardization (ISO)

  • ISO 14155:2020 Plus Redline Clinical investigation of medical devices for human subjects - Good clinical practice
  • ISO 14155:2020 Clinical investigation of medical devices for human subjects — Good clinical practice
  • ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
  • ISO/TS 22990:2019 Traditional Chinese medicine — Categories of clinical terminological system to support the integration of clinical terms from traditional Chinese medicine and Western medicine
  • ISO 14155:2011/cor 1:2011 Clinical investigation of medical devices for human subjects - Good clinical practice; Technical Corrigendum 1
  • ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plants
  • ISO 14155:1996 Clinical investigation of medical devices

Danish Standards Foundation

Association for the Advancement of Medical Instrumentation

  • AAMI/ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
  • ANSI/AAMI/ISO 14155:2020 Clinical investigation of medical devices for human subjects-Good clinical practice
  • AAMI/ISO 14155-2:2003(R2008) Clinical Investigation of Medical Devices for Human Subjects - Part 2: Clinical Investigation Plans
  • ANSI/AAMI/ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
  • AAMI/ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (Includes Erratum, 2011)

Military Standards (MIL-STD)

Korean Agency for Technology and Standards (KATS)

Austrian Standards

German Institute for Standardization

  • DIN EN ISO 14155:2020-12 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • DIN EN ISO 14155:2021-05 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020); German version EN ISO 14155:2020
  • DIN EN ISO 14155:2024 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2024); German and English version prEN ISO 14155:2024
  • DIN EN ISO 14155 E:2018-08 Good Clinical Practice for Clinical Investigation of Medical Devices in Anthropology (Draft)
  • DIN EN ISO 14155 E:2024-09 Draft Document - Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2024); German and English version prEN ISO 14155:2024
  • DIN EN ISO 14155:2018-08 Draft Document - Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2018); German and English version prEN ISO 14155:2018
  • DIN EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
  • DIN EN ISO 14155 E:2018 Draft Document - Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2018); German and English version prEN ISO 14155:2018
  • DIN EN ISO 12487 E:2025-01 Draft Document - Medical electrical equipment - Clinical performance evaluation of clinical thermometers (ISO/DIS 12487:2024); German and English version prEN ISO 12487:2024
  • DIN EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • DIN EN ISO 14155-2 E:2001-08 Clinical Studies of Medical Devices for Human Use Part 2: Clinical Study Protocol (Draft)
  • DIN EN ISO 14155:2021 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020); German version EN ISO 14155:2020

Gosstandart of Russia

  • GOST R 57525-2017 Clinical and economic analysis. General requirements
  • GOST R ISO 14155-2022 Clinical investigation of medical devices for human subjects. Good clinical practice
  • GOST R 59921.1-2022 Artificial intelligence systems in clinical medicine. Part 1. Clinical evaluation
  • GOST R 53022.3-2008 Clinical laboratory technologies. Requirements of quality of clinical laboratory tests. Part 3. Assessment of laboratory tests clinical significance
  • GOST R ISO 14155-2014 Clinical investigation. Good clinical practice
  • GOST R ISO 14155-2-2008 Clinical investigation of medical devices for human subjects. Part 2. Clinical investigation plans
  • GOST R 59921.9-2022 Artificial intelligence systems in clinical medicine. Algorithms for data analysis in clinical physiology. Testing methods. General requirements
  • GOST R 56429-2021 Medical devices. Clinical еvaluation
  • GOST R 56429-2015 Medical devices. Clinical evaluation
  • GOST R 52379-2005 Good clinical practice (GCP)

Standards Norway

  • NS-EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • NS-EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
  • NS-EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans (ISO 14155-2:2003)

Argentine Institute of Standardization

Swedish Institute for Standards

  • SIS 64 41 50-1969 Clinical maximum thermometer
  • SS-EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • SS-EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)

Association Francaise de Normalisation

  • NF S99-201*NF EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
  • NF S94-801:2007 Vaginal reinforcement implant for stress urinary incontinence and/or pelvic organ prolapse repair surgery through vaginal approach - Pre-clinical and clinical tests.
  • NF S99-201/A11*NF EN ISO 14155/A11:2024 Clinical investigation of medical devices for human subjects - Good clinical practice

Japanese Industrial Standards Committee (JISC)

Standard Association of Australia (SAA)

European Committee for Standardization (CEN)

  • EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
  • prEN ISO 14155 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2024)
  • prEN ISO 12487 Medical electrical equipment - Clinical performance evaluation of clinical thermometers (ISO/DIS 12487:2024)

COMMISSION FOR THE STANDARDS, METROLOGY AND QUALITY OF VIETNAM (STAMEQ)

  • TCVN 7740-2-2007 Clinical investigation of medical devices for human subjects.Part 2: Clinical investigation plans

CN-QIYE

American National Standards Institute (ANSI)

American Dental Association

Polski Komitet Normalizacyjny (PKN)

  • PN-EN ISO 14155-2021-02 E Clinical investigation of medical devices for human subjects -- Good clinical practice (ISO 14155:2020)

Indonesia Standards

European Union/Commission

Lithuanian Standards Office

  • LST EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)

Code of Federal Regulations (CFR)

  • CFR 21-862.1-2013 Food and Drugs. Part862:Clinical chemistry and clinical toxicology devices. Section862.1:Scope.