Phases of preclinical research and development
Phases of preclinical research and development, Total:48 items.
The international standard classification for "Phases of preclinical research and development" includes: Medical Sciences and health care facilities in general , Medical equipment in general .
The Chinese standard classification for "Phases of preclinical research and development" includes: Medical science , Medical apparatus and devices in general .
Group Standards of the People's Republic of China
- T/CACM 1126-2018 Traditional Chinese medicine guidelines for the diagnosis and treatment of mental diseases- Premenstrual mental disorder
- T/CAV 001-2023 Terms used in vaccine preclinical research
- T/CACM 1260-2019 Clinical guidelines for diagnosis and treatment of gynecology in TCM Premenstrual syndrome
- T/CAAM 0007-2022 Guidelines for Acupuncture and Moxibustion Clinical Research Registration
- T/CAAM 0011-2020 Specification of record sheets for use of various instruments and equipment for clinical trials of acupuncture and moxibustion in the real world
- T/CACM 015.12-2017 Chinese medicine clinical research verification standards
- T/SDHCST 003-2023 Pre-dose Quality Testing of Test Substances in Non-clinical Studies of the Cell Therapy Medical Products
国家药监局
- YY/T 1754.1-2020 Preclinical animal study of medical devices—Part 1:General considerations
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
未注明发布机构
- DIN EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
- DIN EN ISO 14155-2 E:2001-08 Clinical Studies of Medical Devices for Human Use Part 2: Clinical Study Protocol (Draft)
Inner Mongolia Provincial Standard of the People's Republic of China
- DB15/T 1899-2020 Judgment of primary subclinical ketosis in postpartum dairy cows
National Metrological Technical Specifications of the People's Republic of China
- JJF 1644-2017 The Production of Reference Materials for Clinical Enzymology
SCC
- BS EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects-Clinical investigation plans
- DANSK DS/EN ISO 14155/AC:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
- DANSK DS/ISO 14155:2020 Clinical investigation of medical devices for human subjects – Good clinical practice
- AAMI/ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
- ISO 14155:2020 Plus Redline Clinical investigation of medical devices for human subjects - Good clinical practice
- AS ISO 14155:2002 Clinical investigation of medical devices
- NS-EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans (ISO 14155-2:2003)
- UNE-EN ISO 14155-2:2004 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003)
- 08/30116059 DC BS ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
- AENOR UNE-EN ISO 14155:2012 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
- NS-EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
- DANSK DS/EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
- DANSK DS/EN ISO 14155:2020 Clinical investigation of medical devices for human subjects – Good clinical practice (ISO 14155:2020)
- NS-EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
Korean Agency for Technology and Standards (KATS)
- KS P ISO 14155-2-2007(2012) Clinical investigation of medical devices for human subjects－Part 2：Clinical investigation plans
- KS P ISO 14155-2-2019 Clinical investigation of medical devices for human subjects－Part 2：Clinical investigation plans
American National Standards Institute （ANSI)
- ANSI/HL7 EHRCRFP, R 1-2009 HL7 EHR Clinical Research Functional Profile, Release 1
- ANSI/HL7 V3 PORT, R 1-2004 HL7 Version 3 Standard: Regulated Studies - Periodic Reporting of Clinical Trials Laboratory Results, , Release 1
GSO
- OS GSO ISO 14155:2015 Clinical investigation of medical devices for human subjects -- Good clinical practice
KR-KS
- KS P ISO 14155-2022 Clinical investigation of medical devices for human subjects — Good clinical practice
ES-UNE
- UNE-EN ISO 14155:2021 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
European Committee for Standardization (CEN)
- EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
VN-TCVN
- TCVN 7740-2-2007 Clinical investigation of medical devices for human subjects.Part 2: Clinical investigation plans
German Institute for Standardization
- 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
International Organization for Standardization (ISO)
- ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
US-FCR
- FCR 21 CFR PART 54-2014 FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
- FCR 21 CFR PART 54-2013 FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
- FCR 21 CFR PART 54-2015 FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
British Standards Institution (BSI)
- BS ISO 29943-1:2017 Condoms. Guidance on clinical studies. Male condoms, clinical function studies based on self-reports
- 24/30467406 DC BS EN ISO 14155 Clinical investigation of medical devices for human subjects - Good clinical practice
- BS ISO 29943-2:2017 Condoms. Guidance on clinical studies. Female condoms, clinical function studies based on self-reports
GOST
- GOST R ISO 14155-2022 Clinical investigation of medical devices for human subjects. Good clinical practice
US-HHS
- HHS 21 CFR PART 54 CFR PART 54-2011 FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
Association Francaise de Normalisation
- NF S99-201*NF EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
