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Database: 365,228(8 Aug 2026)

Phase II Clinical Trials

Phase II Clinical Trials, Total:46 items.

The international standard classification for "Phase II Clinical Trials" includes: Dental materials , Laboratory medicine , Medical Sciences and health care facilities in general .

The Chinese standard classification for "Phase II Clinical Trials" includes: Stomatologic device, equipment and material , Sanitation in general .


Group Standards of the People's Republic of China

  • T/CAPA 12-2024 Clinical treatment and long-term management of melasma
  • T/CGCPU 024-2023 Specification for training management of practitioners in clinical trial institution
  • T/CGCPU 006-2019 Phase I Clinical Trial Capacity Evaluation Criteria
  • T/CGCPU 008-2019 General Auditing Standards for Clinical Trials
  • T/CACM 1124~1142-2018 Guidelines for clinical diagnosis and treatment of mental illness in traditional Chinese medicine (II)
  • T/CGCPU 005-2019 Clinical Trial Professional Group Competence Evaluation Criteria
  • 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/SSFSIDC 015-2023 Clinical trial data collection requirements
  • 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 012-2020 File management standards for clinical trial institutions
  • T/CGCPU 014-2020 The practices of chemicals for clinical trials in clinical trial institutions

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 - Medicine

未注明发布机构

  • CLSI GP46-R-2003 Report on the Challenges of Planning Clinical Laboratory Operations During Disasters

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

Professional Standard - Hygiene

  • WS/T 574-2018 Purified reagent water in the clinical laboratory
  • WS/T 834-2024 Clinical application of tests for Toxoplasma gondii

Zhejiang Provincial Standard of the People's Republic of China

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

Jiangsu Provincial Standard of the People's Republic of China

Guangdong Provincial Standard of the People's Republic of China

Gosstandart of Russia

  • 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 14155-2-2008 Clinical investigation of medical devices for human subjects. Part 2. Clinical investigation plans
  • GOST R 52379-2005 Good clinical practice (GCP)

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

GCC Standardization Organization

  • GSO ASTM F3108:2022 Standard Guide for Clinical Outcomes for Clinical Trials and/or Clinical Registries for Knee Reconstructive Surgery

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

Ente Nazionale Italiano di Unificazione

  • UNI EN ISO 14155-2:2004 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans

Association Francaise de Normalisation

US-AAMI

Danish Standards Foundation

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

IT-UNI

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)

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)

German Institute for Standardization

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

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)

Spanish Association for Standardization (UNE)

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

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