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Database: 365,228(8 Aug 2026)

clinical trial completed

clinical trial completed, Total:78 items.

The international standard classification for "clinical trial completed" includes: Dental materials , Medical Sciences and health care facilities in general , Laboratory medicine .

The Chinese standard classification for "clinical trial completed" includes: Stomatologic device, equipment and material , Sanitation in general , Legal medical expert .


Group Standards of the People's Republic of China

  • T/CQAP 3013-2023 Key points for quality inspection of clinical trial data management
  • T/CGCPU 023-2022 Evaluation standard for clinical trial management system document
  • T/CGCPU 005-2019 Clinical Trial Professional Group Competence Evaluation Criteria
  • T/CGCPU 006-2019 Phase I Clinical Trial Capacity Evaluation Criteria
  • T/CGCPU 029-2023 Evaluation requirements of follow-up centers for primary clinical trials
  • T/CGCPU 015-2020 Requirements for Subjects Risk Monitoring system in clinical trials
  • T/CGCPU 008-2019 General Auditing Standards for Clinical Trials
  • T/SHDSGY 066-2023 Inspection service specification of clinical trial research center
  • T/CGCPU 003-2019 Clinical Trial Institution Capacity Evaluation Standards
  • T/CGCPU 006-2023 Specification for competency assessment of phase I clinical trials
  • T/CGCPU 003-2023 Specification for capacity evaluation of clinical trial institutions
  • T/CGCPU 005-2023 Specification for competency assessment of the clinical trial professional group
  • T/CGCPU 024-2023 Specification for training management of practitioners in clinical trial institution
  • T/CGCPU 012-2020 File management standards for clinical trial institutions
  • T/CGCPU 023-2023 Evaluation standard for clinical trial management system document
  • T/CGCPU 013-2020 Ethical Considerations for Subject Pain Management in Clinical Trials
  • T/CGCPU 012-2023 Evaluation specifications for archives management of clinical trial institutions
  • T/CGCPU 022-2023 Evaluation criteria for information management of clinical trials
  • T/CGCPU 014-2020 The practices of chemicals for clinical trials in clinical trial institutions
  • T/CGCPU 020-2022 Guidelines for the management of pain in clinical trial subjects in the pediatric population
  • T/CAV 007-2024 Guidelines for site selection of prophylactic vaccine clinical trial
  • T/SSFSIDC 015-2023 Clinical trial data collection requirements
  • T/CGCPU 022-2022 Evaluation criteria for information management of clinical trials
  • T/CGCPU 024-2022 Specification for training management of practitioners in clinical trial institution

Professional Standard - Medicine

  • YY/T 1305-2015 Clinical trial guideline for titanium and titanium alloy dental implant
  • YY/T 0991-2015 Clinical trial guideline for orthodontic brackets
  • YY/T 0990-2015 Clinical trial guideline for polymer-based dental restorative materials

Jiangsu Provincial Standard of the People's Republic of China

  • DB32/T 4652-2024 Guidelines for the development of multi-center drug clinical trial management systems based on blockchain technology

卫生健康委员会

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

Professional Standard - Hygiene

Zhejiang Provincial Standard of the People's Republic of China

  • DB33/T 903-2013 Classification and coding of clinical laboratory test items

司法部

  • SF/T 0111-2021 Specification of examination in forensic clinical medicine

Professional Standard - Certification and Accreditation

Professional Standard - Public Safety Standards

中华人民共和国国家卫生和计划生育委员会

Professional Standard - Agriculture

RU-GOST R

  • GOST R 53079.3-2008 Medical laboratory technologies. Quality assurance of clinical laboratory tests. Part 3. Rules for interaction between personnel of clinical departments and personnel of clinical-diagnostic laboratory in medical institutions during fulfillment of clinical
  • 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 52379-2005 Good clinical practice (GCP)
  • 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 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 ISO 14155-2014 Clinical investigation. Good clinical practice

GSO

  • GSO ASTM F3108:2022 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Knee Reconstructive Surgery
  • BH GSO ASTM F3108:2023 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Knee Reconstructive Surgery
  • OS GSO 1647:2002 Methods of testing and verification for Clinical electrical thermometers with maximum device

GOST

  • GOST R ISO 14155-2-2008 Clinical investigation of medical devices for human subjects. Part 2. Clinical investigation plans
  • GOST R 70355-2022 Specialized food products. General requirements for preclinical tests on laboratory animals

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
  • ASTM E2045-99 Standard Practice for Detailed Clinical Observations of Test Animals

Association Francaise de Normalisation

US-AAMI

IT-UNI

Danish Standards Foundation

  • DS/EN ISO 14155:2013 Clinical investigation of medical devices for human subjects - Good clinical practice

European Committee for Standardization (CEN)

  • EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)

British Standards Institution (BSI)

  • BS EN ISO 14155:2011 Clinical investigation of medical devices for human subjects. Good clinical practice

PL-PKN

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

German Institute for Standardization

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

Lithuanian Standards Office

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

AT-ON

  • OENORM 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)

Korean Agency for Technology and Standards (KATS)

  • KS B ISO 13041-6:2012 Test conditions for numerically controlled turning machines and turning centres-Part 6:Accuracy of a finished test piece
  • KS B ISO 13041-6:2014 Test conditions for numerically controlled turning machines and turning centres — Part 6: Accuracy of a finished test piece

ZA-SANS

  • SANS 16037:2003 Rubber condoms for clinical trials - Measurement of physical properties

Canadian General Standards Board (CGSB)

American National Standards Institute (ANSI)

  • ANSI/HL7 V3 PORT, R 1-2004 HL7 Version 3 Standard: Regulated Studies - Periodic Reporting of Clinical Trials Laboratory Results, , Release 1

ASHRAE - American Society of Heating@ Refrigerating and Air-Conditioning Engineers@ Inc.