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In vivo clinical diagnostic reagents
In vivo clinical diagnostic reagents, Total:31 items.
In the international standard classification, In vivo clinical diagnostic reagents involves: Laboratory medicine, Medical equipment, Medical sciences and health care facilities in general.
General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, In vivo clinical diagnostic reagents
Professional Standard - Medicine, In vivo clinical diagnostic reagents
- YY/T 1227-2014 In vitro diagnostic reagent (kit) nomenclature for clinical chemistry
- YY/T 0688.2-2010 Clinical laboratory testing and in vitro diagnostic test systems.Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility devices.Part 2 : Evaluation of performance of antimicrobial susceptibility test devi
中华人民共和国国家卫生和计划生育委员会, In vivo clinical diagnostic reagents
- WS/T 124-1999 Inspection criteria of the quality of clinical chemistry in vitro diagnostic kits.General guideline
RU-GOST R, In vivo clinical diagnostic reagents
- GOST R 51352-1999 Kits of reagents for clinical laboratory diagnostics. Test methods
- GOST R 51088-1997 Kits of reagents for clinical laboratory diagnostics. General specifications
- GOST R ISO 16256-2015 Clinical laboratory testing and in vitro diagnostic test systems. Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
- GOST R 53133.1-2008 Clinical laboratory technologies. Quality control of clinical laboratory tests. Part 1. Limits of allowable errors of the results of the analyte measurements in clinical-diagnostics laboratories
- GOST R 55991.7-2014 In vitro diagnostics medical devices. Part 7. Automatic analyzers for general clinical tests. Technical requirements for public procurement
Shanxi Provincial Standard of the People's Republic of China, In vivo clinical diagnostic reagents
- DB14/T 2254-2020 Regulations on cold storage and freezing management of clinical in vitro diagnostic reagents in medical institutions
KR-KS, In vivo clinical diagnostic reagents
- KS P ISO 19001-2017(2022) In virto diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
- KS P ISO 16256-2022 Clinical laboratory testing and in vitro diagnostic test systems — Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infec
Korean Agency for Technology and Standards (KATS), In vivo clinical diagnostic reagents
- KS P ISO TR 18112-2009(2014) Clinical laboratory testing and in vitro diagnostic test systems－In vitro diagnostic medical devices for professional use－Summary of regulatory requirements for information supplied by the manufacture
Association Francaise de Normalisation, In vivo clinical diagnostic reagents
- NF S92-012*NF EN ISO 16256:2013 Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases
- NF S92-012*NF EN ISO 16256:2021 Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
International Organization for Standardization (ISO), In vivo clinical diagnostic reagents
- ISO 16256:2012 Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
- ISO 16256:2021 Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
British Standards Institution (BSI), In vivo clinical diagnostic reagents
- BS EN ISO 16256:2012 Clinical laboratory testing and in vitro diagnostic test systems. Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases
- BS ISO 20916:2019 In vitro diagnostic medical devices. Clinical performance studies using specimens from human subjects. Good study practice
- BS EN ISO 16256:2021 Tracked Changes. Clinical laboratory testing and in vitro diagnostic test systems. Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
Professional Standard - Agriculture, In vivo clinical diagnostic reagents
- 1342药典 化学药和生物制品卷-2010 Chapter 18 Biological Products 8. In Vivo Diagnostic Reagent Sik Test Toxin
- 1341药典 化学药和生物制品卷-2010 Chapter 18 Biological Products 8. In Vivo Diagnostic Reagent Brucella Pure Protein Derivatives
- 1340药典 化学药和生物制品卷-2010 Chapter 18 Biological Products 8. In Vivo Diagnostic Reagent BCG Pure Protein Derivatives
- 1339药典 化学药和生物制品卷-2010 Chapter 18 Biological Products 8. In Vivo Diagnostic Reagent Tuberculin Pure Protein Derivatives
BE-NBN, In vivo clinical diagnostic reagents
- NBN-EN 375-1992 In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for professional use
AENOR, In vivo clinical diagnostic reagents
- UNE-EN ISO 16256:2013 Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012)
ES-UNE, In vivo clinical diagnostic reagents
- UNE-EN ISO 16256:2021 Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021) (Endorsed by Asociac...
German Institute for Standardization, In vivo clinical diagnostic reagents
- DIN EN ISO 16256:2022-02 Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021); German version EN I...
国家药监局, In vivo clinical diagnostic reagents
- YY/T 1728-2021 Reference method for in vitro activity testing of yeast-like fungal antimicrobials related to systemic infectious diseases for clinical laboratory testing and in vitro diagnostics
European Committee for Standardization (CEN), In vivo clinical diagnostic reagents
- EN ISO 16256:2021 Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021)
- EN ISO 16256:2012 Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012)