diagnostic evaluation
diagnostic evaluation, Total:63 items.
The international standard classification for "diagnostic evaluation" includes: Laboratory medicine , Soil quality. Pedology .
The Chinese standard classification for "diagnostic evaluation" includes: Medical laboratory equipment , School sanitation , Medical apparatus and devices in general , Soil and fertilizer in general .
Military Standard of the People's Republic of China-General Armament Department
- GJB 10102-2021 Diagnostic evaluation method of spacecraft control system
国家药品监督管理局
- YY/T 1579-2018 In vitro diagnostic medical devices—Evaluation of stability of in vitro diagnostic reagents
中华人民共和国国家卫生和计划生育委员会
- WS/T 200-2001 Diagnosis and treatment evaluation for strabismus of children and adolescents
Group Standards of the People's Republic of China
- T/CI 310-2024 Performance evaluation of blockers in raw materials for in vitro diagnostic products
- T/BSRS 093-2023 Standard review plans for environmental impact assessment document of fluorine-18 nuclide diagnostic project
- T/ITS 0223.3-2023 Traffic operation status evaluation diagnosis and governance system for intelligent and connected intersections—Part 3: Monitor and diagnosis goverance
- T/BSRS 091-2023 Standard review plans for environmental impact assessment document of technetium-99m radiopharmaceutical preparation and diagnosis project
- T/GDAQI 84-2022 Methodological comparison and evaluation of the accuracy of in vitro diagnostic reagents
- T/YNBX 140-2024 Energy-saving diagnosis technology and evaluation requirements for cement production enterprises
- T/GDC 155-2022 Performance evaluation method of Artificial Intelligence Aided judgment algorithm for ECG diagnosis equipment
- T/SCGS 313001-2023 Standards for testing and performance evaluation of intelligent auxiliary diagnostic software for gastric tumors
- T/CNMIA 0032-2021 Competence Evaluation Criteria for Independent Pathological Diagnosis Center/Pathology Laboratory
国家药监局
- YY/T 1789.2-2021 In vitro diagnostic test systems-Performance evaluation method-Part 2:Trueness
- YY/T 1789.1-2021 In vitro diagnostic test systems-Performance evaluation method-Part 1:Precision
Professional Standard - Hygiene
- WS/T 201-2001 Diagnosis and treatment evaluation for amblyopia of children and adolescents
Professional Standard - Medicine
- YY/T 1789.6-2023 In vitro diagnostic test systems―Performance evaluation method―Part 6:Precision, diagnostic sensitivity and specificity of qualitative reagents
- YY/T 1789.5-2023 In vitro diagnostic test systems--Performance evaluation method一Part 5:Analytical specificity
Professional Standard - Agriculture
- NY/T 1749-2009 Soil fertility diagnosis and evaluation method of farmland in Southern China
Professional Standard - Commodity Inspection
- SN/T 2435-2010 Protocol of quality assessment on the diagnostic kits used in entry-exit animal quarantine
German Institute for Standardization
- DIN EN ISO 23640:2015-12 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2015 / Note: DIN EN ISO 23640 (2013-09) remains valid alongside this standard until 2018-06-30.
- DIN EN 13612:2002-08 Performance evaluation of in vitro diagnostic medical devices; German version EN 13612:2002, German and English texts
- DIN EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices; German version EN 13612:2002, German and English texts
SCC
- DANSK DS/EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
- DANSK DS/EN 13612/AC:2003 Performance evaluation of in vitro diagnostic medical devices
- NS-EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
- DANSK DS/EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
- AENOR UNE-EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices.
- AENOR UNE-EN 13612/AC:1970 Performance evaluation of in vitro diagnostic medical devices.
- NS-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
- AENOR UNE-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
- NS-EN ISO 23640:2011 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
- NS-EN ISO 23640:2013 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
- DIN EN ISO 23640 E:2013 Draft Document - In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2013
Association Francaise de Normalisation
- NF EN ISO 23640:2015 In vitro diagnostic medical devices - Assessment of the stability of in vitro diagnostic reagents
- NF EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
- NF S92-025*NF EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
- NF S92-032*NF EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
- NF S92-032:2014 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
British Standards Institution (BSI)
- BS EN ISO 23640:2015 In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
- BS EN ISO 23640:2013 In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
- BS EN ISO 23640:2011 In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
- BS EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
ES-UNE
- UNE-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
- UNE-EN 13612/AC:2003 Performance evaluation of in vitro diagnostic medical devices.
GOSTR
- GOST R EN 13612-2010 Performance evaluation of in vitro diagnostic medical devices
Korean Agency for Technology and Standards (KATS)
- KS P ISO 23640:2013 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
- KS P 1977-2018 Protocol for evaluation of qualitative test performance in in-vitro diagnostic medical laboratory
- KS P 1800-2013 Protocol for evaluation of matrix effects in in-vitro diagnostic test
- KS P 1975-2023 Protocol for evaluation of precision performance of the quantitative test in in-vitro diagnostic medical laboratory
- KS P ISO 23640:2019 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
- KS P 1975-2018 Protocol for evaluation of precision performance of the quantitative test in in-vitro diagnostic medical laboratory
AENOR
- UNE-EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices.
- UNE-EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
European Committee for Standardization (CEN)
- EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
- EN ISO 23640:2011 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents [Superseded: CEN EN 13640]
- EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
KR-KS
- KS P ISO 23640-2019 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
- KS P 2170-2022 Protocol for analytical performance evaluation of infectious disease molecular diagnosis in in-vitro diagnostic medical laboratory
International Organization for Standardization (ISO)
- ISO 23640:2011 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
RU-GOST R
- GOST 27905.2-1988 Electrical insulation systems. Evaluation of performances evaluation, ageing mechanism, diagnostic procedures
- GOST R ISO 18436-1-2015 Condition monitoring and diagnostics of machines. Requirements for qualification and assessment of personnel. Part 1. Requirements for assessment bodies and the assessment process
- GOST R ISO 18436-2-2015 Condition monitoring and diagnostics of machines. Requirements for qualification and assessment of personnel. Part 2. Vibration condition monitoring and diagnostics
CN-ZY
- ZY/T 10-2024 General rules for the formulation and revision of the diagnosis and efficacy evaluation standards of TCM diseases and syndromes
Safety Evaluation,Equipment Safety Evaluation,Equipment Safety Evaluation,Reliability Evaluation,Effectiveness evaluation,Evaluation of Toxicity Effectiveness,Safety Evaluation,In vitro diagnostic clinical evaluation,In vitro diagnostic clinical evaluation,Reliability Evaluation,Durability Evaluation,Durability Evaluation,environmental assessment,Compliance Evaluation,diagnostic evaluation,Uniformity evaluation,Integrity Evaluation,Applicability evaluation,Diagnostic Performance Evaluation of Clinical Diagnostic Tests,Diagnosability