Medical Device Clinical Research
Medical Device Clinical Research, Total:27 items.
The international standard classification for "Medical Device Clinical Research" includes: .
The Chinese standard classification for "Medical Device Clinical Research" includes: .
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- 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)
SCC
- AS ISO 14155:2002 Clinical investigation of medical devices
- BS EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects-Clinical investigation plans
- BS EN 540:1993 Clinical investigation of medical devices for human subjects
- NS-EN 540:1993 Clinical investigation of medical devices for human subjects
- BS EN ISO 14155-1:2009 Clinical investigation of medical devices for human subjects-General requirements
- 08/30116059 DC BS ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
- DANSK DS/EN ISO 14155-1:2009 Clinical investigation of medical devices for human subjects - Part 1: General requirements
- 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)
Danish Standards Foundation
- DS/EN 540:1993 Clinical investigation of medical devices for human subjects
GSO
- OS GSO ISO 14155:2015 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 14155-1-2007(2012) Clinical investigation of medical devices for human subjects－Part 1：General requirements
German Institute for Standardization
- 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
- ISO 14155:2011/cor 1:2011 Clinical investigation of medical devices for human subjects - Good clinical practice; Technical Corrigendum 1
British Standards Institution (BSI)
- 24/30467406 DC BS EN ISO 14155 Clinical investigation of medical devices for human subjects - Good clinical practice
- BS EN 540:1993(1998) Clinicalinvestigationof medical devices for human subjects
VN-TCVN
- TCVN 7740-2-2007 Clinical investigation of medical devices for human subjects.Part 2: Clinical investigation plans
European Committee for Standardization (CEN)
- EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
- prEN 540-1992 Clinical investigation of medical devices for human subjects
- EN 540:1993 Clinical Investigation of Medical Devices for Human Subjects Superseded by EN ISO 14155-1:2003
Association Francaise de Normalisation
- NF S99-201:1993 Clinical investigation of medical devices for human subjects.
NL-NEN
- NEN-EN 540-1994 Clinical investigation of medical devices for human subjects
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