Medical device non-clinical
Medical device non-clinical, Total:83 items.
The international standard classification for "Medical device non-clinical" includes: Medical equipment in general .
The Chinese standard classification for "Medical device non-clinical" includes: Medical apparatus and devices in general .
Professional Standard - Medicine
- YY/T 0297-1997 Clinical investigation of medical devices
Group Standards of the People's Republic of China
- T/CACM 1138-2018 Traditional Chinese medicine guidelines for the diagnosis and treatment of mental diseases- Non-organic insomnia
- T/CGCPU 026-2023 Design specifications for clinical trial protocol of cardiovascular interventional medical devices
国家药监局
- YY/T 1754.1-2020 Preclinical animal study of medical devices—Part 1:General considerations
Standard Association of Australia (SAA)
- AS ISO 14155:2002 Clinical investigation of medical devices
- AS ISO 14155.1:2004 Clinical investigations of medical devices for human subjects - General requirements
RU-GOST R
- GOST R 56429-2015 Medical devices. Clinical evaluation
- GOST R ISO 14155-2014 Clinical investigation. Good clinical practice
GSO
- OS GSO ISO 14155:2015 Clinical investigation of medical devices for human subjects -- Good clinical practice
- GSO ISO 14155:2015 Clinical investigation of medical devices for human subjects -- Good clinical practice
SCC
- BS EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects-Clinical investigation plans
- ISO 14155:2020 Plus Redline Clinical investigation of medical devices for human subjects - Good clinical practice
- DANSK DS/EN ISO 14155/AC:2011 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
- DANSK DS/ISO 14155:2020 Clinical investigation of medical devices for human subjects – Good clinical practice
- 08/30116059 DC BS ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
- BS EN 540:1993 Clinical investigation of medical devices for human subjects
- NS-EN 540:1993 Clinical investigation of medical devices for human subjects
- NS-EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
- NS-EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
- DANSK DS/EN ISO 14155:2020 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)
- BS EN ISO 14155-1:2009 Clinical investigation of medical devices for human subjects-General requirements
- 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
- AAMI ST35:2003 Safe Handling and Biological Decontamination of Reusable Medical Devices in Health Care Facilities and in Nonclinical Settings
- NS-EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans (ISO 14155-2:2003)
- AAMI/ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (Includes Erratum, 2011)
- DANSK DS/EN ISO 14155-1:2009 Clinical investigation of medical devices for human subjects - Part 1: General requirements
- DANSK DS/EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
European Committee for Standardization (CEN)
- prEN 540-1992 Clinical investigation of medical devices for human subjects
- EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
- EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
- EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
- EN ISO 14155-2:2003 Clinical Investigation of Medical Devices for Human Subjects - Part 2: Clinical Investigation Plans ISO 14155-2:2003
- EN 540:1993 Clinical Investigation of Medical Devices for Human Subjects Superseded by EN ISO 14155-1:2003
KR-KS
- KS P ISO 14155-2022 Clinical investigation of medical devices for human subjects — Good clinical practice
Association Francaise de Normalisation
- NF S99-201:1993 Clinical investigation of medical devices for human subjects.
- NF S99-201*NF EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
British Standards Institution (BSI)
- BS EN 540:1993(1998) Clinicalinvestigationof medical devices for human subjects
- 24/30467406 DC BS EN ISO 14155 Clinical investigation of medical devices for human subjects - Good clinical practice
- BS EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Clinical investigation plans
- 18/30344902 DC BS EN ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
- BS EN ISO 14155:2011 Clinical investigation of medical devices for human subjects. Good clinical practice
- BS EN ISO 14155:2020 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)
- 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)
NL-NEN
- NEN-EN 540-1994 Clinical investigation of medical devices for human subjects
German Institute for Standardization
- DIN EN 540:1993 Clinical testing of medical devices on humans
- 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 14155:2021-05 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020); German version EN ISO 14155:2020
- DIN EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
- 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
- DIN EN 540 Berichtigung 1:1998 Clinical testing of medical devices on humans; German version EN 540: 1993
Danish Standards Foundation
- DS/EN 540:1993 Clinical investigation of medical devices for human subjects
- DS/EN ISO 14155:2013 Clinical investigation of medical devices for human subjects - Good clinical practice
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
- KS P ISO 14155-2:2007 Clinical investigation of medical devices for human subjects-Part 2:Clinical investigation plans
- KS P ISO 14155-1-2007(2012) Clinical investigation of medical devices for human subjects-Part 1:General requirements
- KS P ISO 14155-1-2019 Clinical investigation of medical devices for human subjects-Part 1:General requirements
International Organization for Standardization (ISO)
- ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
- ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plants
- ISO 14155:2011/cor 1:2011 Clinical investigation of medical devices for human subjects - Good clinical practice; Technical Corrigendum 1
- ISO 14155:1996 Clinical investigation of medical devices
GOST
- GOST R ISO 14155-2022 Clinical investigation of medical devices for human subjects. Good clinical practice
- GOST R ISO 14155-2-2008 Clinical investigation of medical devices for human subjects. Part 2. Clinical investigation plans
- GOST R 56429-2021 Medical devices. Clinical еvaluation
IT-UNI
- EC 1-2020 UNI EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
- UNI EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
US-AAMI
- ANSI/AAMI/ISO 14155:2020 Clinical investigation of medical devices for human subjects-Good clinical practice
- ANSI/AAMI/ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
- AAMI TIR49-2013 Design of training and instructional materials for medical devices used in non-clinical environments
VN-TCVN
- TCVN 7740-2-2007 Clinical investigation of medical devices for human subjects.Part 2: Clinical investigation plans
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)
PL-PKN
- PN-EN ISO 14155-2021-02 E Clinical investigation of medical devices for human subjects -- Good clinical practice (ISO 14155:2020)
BE-NBN
- NBN-EN 540-1993 Clinical investigation of medical devices for human subjects
American Society for Testing and Materials (ASTM)
- ASTM D817-96(2004)e1 Standard Test Methods of Testing Cellulose Acetate Propionate and Cellulose Acetate Butyrate
- ASTM D8179-18 Standard Guide for Characterizing Detergents for the Cleaning of Clinically-used Medical Devices
Institute of Electrical and Electronics Engineers (IEEE)
- Ethically Aligned Design - A Vision for Prioritizing Human Well-being with Autonomous and Intelligen Ethically Aligned Design - A Vision for Prioritizing Human Well-being with Autonomous and Intelligent Systems
non-clinical research,Medical device non-clinical,Non-clinical medical devices,Medical device non-clinical,Nonclinical Research Medical Devices,Medical device non-clinical research,Non-clinical evaluation of medical devices,,Dental non-clinical,non-clinical environment,non-clinical data,bacterianon-clinical,Medical device non-clinical research,Non-clinical evaluation of medical devices,non-clinical market,clinical medical equipment clinical,non-clinical registration,nonclinical evaluation,Non-registered clinical,nonclinical evaluation