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Clinical + Trial

Clinical + Trial, Total:82 items.

In the international standard classification, Clinical + Trial involves: Medical sciences and health care facilities in general, Pharmaceutics, Test conditions and procedures in general, Dentistry, Hospital equipment, Quality, Birth control. Mechanical contraceptives, Terminology (principles and coordination), Medical equipment, Laboratory medicine, Construction materials.


Group Standards of the People's Republic of China, Clinical + Trial

  • T/CGCPU 014-2020 The practices of chemicals for clinical trials in clinical trial institutions
  • T/SSFSIDC 015-2023 Clinical trial data collection requirements
  • T/CGCPU 008-2019 General Auditing Standards for Clinical Trials
  • T/CGCPU 006-2019 Phase I Clinical Trial Capacity Evaluation Criteria
  • T/CGCPU 012-2020 File management standards for clinical trial institutions
  • T/CGCPU 024-2023 Specification for training management of practitioners in clinical trial institution
  • T/CGCPU 003-2023 Specification for capacity evaluation of clinical trial institutions
  • T/CGCPU 024-2022 Specification for training management of practitioners in clinical trial institution
  • 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 005-2019 Clinical Trial Professional Group Competence Evaluation Criteria
  • T/CGCPU 022-2022 Evaluation criteria for information management of clinical trials
  • T/CGCPU 005-2023 Specification for competency assessment of the clinical trial professional group
  • T/CGCPU 022-2023 Evaluation criteria for information management of clinical trials
  • T/CGCPU 029-2023 Evaluation requirements of follow-up centers for primary clinical trials
  • T/CGCPU 012-2023 Evaluation specifications for archives management of clinical trial institutions
  • T/CGCPU 023-2022 Evaluation standard for clinical trial management system document
  • T/CQAP 3013-2023 Key points for quality inspection of clinical trial data management
  • T/CGCPU 023-2023 Evaluation standard for clinical trial management system document
  • T/SHDSGY 066-2023 Inspection service specification of clinical trial research center
  • T/CAV 007-2024 Guidelines for site selection of prophylactic vaccine clinical trial
  • T/CGCPU 002-2023 Evaluation standard of centralized management of clinical investigational product
  • T/CGCPU 020-2022 Guidelines for the management of pain in clinical trial subjects in the pediatric population
  • T/CGCPU 015-2020 Requirements for Subjects Risk Monitoring system in clinical trials
  • T/CGCPU 013-2020 Ethical Considerations for Subject Pain Management in Clinical Trials
  • T/CACM 1333.3-2019 Technical guidelines for the design and evaluation of traditional Chinese medicine clinical trials for pediatric common diseases Part 3: Functional abdominal pain
  • T/CAV 009-2024 Quality control standards for on-site implementation of vaccine clinical trials
  • T/CGCPU 027-2023 Design specifications for clinical research protocol of immunotherapy
  • T/SHSPS 001-2024 Standards for Management and Competency Assessment of Clinical Trial Coordinators (Shanghai)
  • T/SHSPS 002-2024 Standards for the management and competency evaluation of clinical trial monitors (Shanghai)
  • T/CACM 1333.4-2019 Technical guidelines for the design and evaluation of traditional Chinese medicine clinical trials for pediatric series of common diseases Part 4: Diarrhea in children
  • T/CACM 1333.2-2019 Technical guidelines for the design and evaluation of traditional Chinese medicine clinical trials for common diseases in the pediatric system Part 2: functional constipation
  • T/SHQAP 001-2023 Guidelines for the Construction of Quality Management Systems for Drug Clinical Trial Sponsors
  • T/CAAM 0004-2023 Guidelines for setting up and reporting sham acupuncture controls in acupuncture clinical trials
  • T/CACM 1333.1-2019 Technical guidelines for the design and evaluation of traditional Chinese medicine clinical trials for common diseases in the pediatric system Part 1: Anorexia
  • T/CGCPU 026-2023 Design specifications for clinical trial protocol of cardiovascular interventional medical devices

GOST, Clinical + Trial

  • GOST R ISO 14155-2-2008 Clinical investigation of medical devices for human subjects. Part 2. Clinical investigation plans

RU-GOST R, Clinical + Trial

Professional Standard - Medicine, Clinical + Trial

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

Jiangsu Provincial Standard of the People's Republic of China, Clinical + Trial

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

Canadian General Standards Board (CGSB), Clinical + Trial

ZA-SANS, Clinical + Trial

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

GSO, Clinical + Trial

  • 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
  • BH GSO ASTM F3037:2022 Standard Guide for Clinical Trial Design for Hip Replacement Systems (HRSs)
  • GSO ASTM F3037:2021 Standard Guide for Clinical Trial Design for Hip Replacement Systems (HRSs)
  • OS GSO ISO 16037:2009 Rubber condoms for clinical trials – Measurement of physical properties

Association Francaise de Normalisation, Clinical + Trial

Hunan Provincial Standard of the People's Republic of China, Clinical + Trial

  • DB43/T 2135-2021 Technical Service Specifications for the Recruitment and Management of Drug Clinical Trial Subjects

US-AAMI, Clinical + Trial

IT-UNI, Clinical + Trial

Danish Standards Foundation, Clinical + Trial

  • DS/EN ISO 14155:2013 Clinical investigation of medical devices for human subjects - Good clinical practice
  • DS/ISO 16037:2002 Rubber condoms for clinical trials - Measurement of physical properties

Korean Agency for Technology and Standards (KATS), Clinical + Trial

KR-KS, Clinical + Trial

American Society for Testing and Materials (ASTM), Clinical + Trial

  • 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 F3037-15 Standard Guide for Clinical Trial Design for Hip Replacement Systems (HRSs)

International Organization for Standardization (ISO), Clinical + Trial

  • ISO 16037:2002 Rubber condoms for clinical trials - Measurement of physical properties

SCC, Clinical + Trial

Anhui Provincial Standard of the People's Republic of China, Clinical + Trial

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

AENOR, Clinical + Trial

  • UNE-EN ISO 14155:2012 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)

PL-PKN, Clinical + Trial

  • 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, Clinical + Trial

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

Lithuanian Standards Office , Clinical + Trial

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

AT-ON, Clinical + Trial

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

Professional Standard - Agriculture, Clinical + Trial

European Committee for Standardization (CEN), Clinical + Trial

  • 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), Clinical + Trial

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




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