r in medicine

r in medicine, Total:251 items.

The international standard classification for "r in medicine" includes: Information sciences , IT applications in health care technology , Health care technology (Vocabularies) .

The Chinese standard classification for "r in medicine" includes: Medical apparatus and devices in general , Hygiene, safety and labor protection , Pharmaceutical in general .

Group Standards of the People's Republic of China

T/CARDTCM CARDTCM006-2022 TCM True Qi Movement Health Care Teaching Standards
T/WFCMS SCM3-2009 World Standard of Chinese Medicine Undergraduate(Pre-CMD)Education
T/ACSC 01-2022 Standard for the construction of assisted reproductive medicine centers
T/SXS 054-2024 Technical specification for plant protection teaching of Chinese medicinal materials
T/WFCMS SCM10-2012 World Core Courses of Chinese Medicine Specialty
T/HARACM 0013-2024 Chinese Medicine academic Co construction unit Management standards
T/CSRS CSRS-2022 Guidelines for the Construction of Sleep Medicine Centers in China
T/QDAS 140-2025 Construction and service specifications of simulation medical center
T/CHAS 10-2-16-2019 Quality and safety management of Chinese hospital Part 2-16: Patients service——Medical image
T/CIATCM 039-2019 Functional specification of the management information system for education in the hospitals of Traditional Chinese Medicine
T/CMAM A10-2021 Chinese Association of Ethnic Medicine Yao Medicine Terminology Standards
T/HARACM 0007-2023 TCM medical record evaluation tool based on evidence-based medicine PICO model
T/CNMIA 0017-2020 Evaluation of the ability of independent medical imaging centers run by society
T/GZYJNY 05-2018 Agriculture of traditional Chinese medical science

未注明发布机构

AAMI TIR55-2014(2017) Human factors engineering for processing medical devices
CLSI MM09-A2-2014 Nucleic Acid Sequencing Methods in Diagnostic Laboratory Medicine; Approved Guideline—Second Edition
AAMI ST58-2018 Application of chemical sterilization and high-level disinfection in medical institutions
CLSI C52-2017 Application of Toxicology and Drug Testing in Medical Laboratories

Professional Standard - Public Safety Standards

GA/T 167-2019 Forensic medicine—Specifications for examination of poisoning deaths

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

GB/T 43278-2023 Medical laboratories—Application of risk management to medical laboratories
GB/T 42467.6-2023 Clinical terminology of traditional Chinese medicine—Part 6:Gynecology
GB/T 38327-2019 Health informatics—Classification of traditional Chinese medicine data sets
GB/T 42467.2-2023 Clinical terminology of traditional Chinese medicine—Part 2：External medicine
GB/T 42467.7-2023 Clinical terminology of traditional Chinese medicine—Part 7:Pediatrics
GB/T 42467.8-2023 Clinical terminology of traditional Chinese medicine—Part 8:Ophthalmology
GB 16361-1996 Radiological protection standards for the patient in clinical nuclear medicine
GB/T 40670-2021 Guidelines for establishment and development of traditional Chinese medical thesauri
GB/T 16886.18-2022 Biological evaluation of medical devices—Part 18: Chemical characterization of medical device materials within a risk management process
GB/T 42467.1-2023 Clinical terminology of traditional Chinese medicine—Part 1：Internal medicine
GB/T 38324-2019 Health informatics -- Semantic network framework of traditional Chinese medicine language system

Hebei Provincial Standard of the People's Republic of China

DB13/T 5313-2020 Medical Imaging Diagnosis Process and Standards for Stroke

Professional Standard - Hygiene

WS/T 544-2017 Medical digital imaging Chinese packaging and communication specifications

Professional Standard - Chemical Industry

HG 3-1305-1980 Chemical Reagent Alizarin Yellow R

PH-BPS

PNS ISO 19465:2021 Traditional Chinese medicine - Categories of traditional Chinese medicine (TCM) clinical terminological systems

European Committee for Standardization (CEN)

DD ENV 12623-1997 Medical Informatics - Media Interchange in Medical Imaging Communications (MI-MEDICOM)
EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
DD ENV 12017-1997 Medical Informatics - Medical Informatics Vocabulary (MIVoc)
DD ENV 12052-1997 Medical Informatics - Medical Imaging Communication (MEDICOM)
EN ISO 10993-18:2020/prA1 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
CEN ISO/TR 12296:2013 Ergonomics - Manual handling of people in the healthcare sector
DD ENV 12611-1997 Medical Informatics - Categorial Structure of Systems of Concepts - Medical Devices
DD ENV 12967-1-1998 Medical Informatics - Healthcare Information System Architecture (HISA) - Part 1: Healthcare Middleware Layer

British Standards Institution (BSI)

BS DD ENV 12623:1998 Medical informatics. Media interchange in Medical imaging communications (MI-MEDICOM)
PD ISO/TS 16277-1:2015 Health informatics. Categorial structures of clinical findings in traditional medicine. Traditional Chinese, Japanese and Korean medicine
BS EN ISO 22367:2020 Medical laboratories. Application of risk management to medical laboratories
BS DD ENV 12967-1:1998 Medical informatics. Healthcare Information System Architecture (HISA)-Healthcare middleware layer
DD ENV 12537-1:1998 Medical informatics. Registration of information objects used for EDI in healthcare.. The register
19/30391662 DC BS ISO 22367. Medical laboratories. Application of risk management to medical laboratories
25/30479947 DC BS EN ISO 22367 Medical laboratories - Application of risk management to medical laboratories
BS DD ENV 12537-2:1998 Medical informatics. Registration of information objects used for EDI in healthcare.-Procedures for the registration of information objects used in electronic data interchange (EDI) in healthcare
BS PD ISO/TS 16277-1:2015 Health informatics. Categorial structures of clinical findings in traditional medicine. Traditional Chinese, Japanese and Korean medicine
BS EN ISO 10993-18:2020+A1:2023 Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
PD ISO/TS 23824:2024 Medical laboratories — Guidance on application of ISO 15189 in anatomic pathology
BS PD ISO/TS 23824:2024 Medical laboratories. Guidance on application of ISO 15189 in anatomic pathology
BS PD ISO/TS 18790-1:2015 Health informatics. Profiling framework and classification for Traditional Medicine informatics standards development. Traditional Chinese Medicine
BS PD ISO/TS 17948:2014 Health informatics. Traditional Chinese medicine literature metadata
DD ENV 13609-2:2000 Healthcare informatics. Messages for maintenance of supporting information in healthcare systems. Updating of medical laboratory-specific information
BS ISO 18665:2015 Traditional Chinese medicine. Herbal decoction apparatus
BS EN ISO 10993-18:2020 Biological evaluation of medical devices Part 18 : Chemical characterization of medical device materials within a risk management process
BS DD ENV 12017:1998 Medical informatics. Medical informatics vocabulary (MIVoc)
BS DD ENV 12052:1998 Medical informatics. Medical imaging communication (MEDICOM)
BS PD ISO/TS 17938:2014 Health informatics. Semantic network framework of traditional Chinese medicine language system
PD ISO/TS 17948:2014 Health informatics. Traditional Chinese medicine literature metadata
PD ISO/TS 18790-1:2015 Health informatics. Profiling framework and classification for Traditional Medicine informatics standards development. Traditional Chinese Medicine
DD ENV 12435-2000 Medical informatics. Expression of results of measurements in health sciences
DD ENV 12610:1998 Medical informatics. Medical product identification
18/30358832 DC BS EN ISO 10993-18. Biological evaluation of medical devices. Part 18. Chemical characterization of medical device materials within a risk management process
PD ISO/TS 9321:2024 Health informatics — General requirements of multi-centre medical data collaborative analysis
BS EN ISO 12894:2001 Ergonomics of the thermal environment - Medical supervision of individuals exposed to extreme hot or cold environments
DD ENV 12611:1998 Medical informatics. Categorical structure of systems of concepts. Medical devices
21/30439273 DC BS EN ISO 10993-18 AMD1. Biological evaluation of medical devices - Part 18. Chemical characterization of medical device materials within a risk management process
BS EN 16844:2017+A1:2018 Aesthetic medicine services. Non-surgical medical treatments

Korean Agency for Technology and Standards (KATS)

KS X ISO TS 16277-1-2017 Health informatics ― Categorial structures of clinical findings in traditional medicine ― Part 1: Traditional Chinese, Japanese and Korean medicine
KS X ISO TS 16277-1-2022 Health informatics ― Categorial structures of clinical findings in traditional medicine ― Part 1: Traditional Chinese, Japanese and Korean medicine
KS X ISO TS 16277-1:2017 Health informatics ― Categorial structures of clinical findings in traditional medicine ― Part 1: Traditional Chinese, Japanese and Korean medicine
KS X ISO TS 16277-1-2017(2022) Health informatics ― Categorial structures of clinical findings in traditional medicine ― Part 1: Traditional Chinese, Japanese and Korean medicine
KS P ISO 10993-18-2021 Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
KS P ISO 10993-18:2021 Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
KS X ISO TR 24291-2023 Health informatics Applications of machine learning technologies in imaging and other medical applications
KS P ISO 10993-18-2024 Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
KS P ISO 22367-2023 Medical laboratories — Application of risk management to medical laboratories
KS B ISO 2541-2018 Centre drills for centre holes with radius form — Type R

International Laboratory Accreditation Cooperation

ILAC G19:06/2022 Modules in a Forensic Science Process

International Organization for Standardization (ISO)

ISO 22367:2020 Medical laboratories — Application of risk management to medical laboratories
IWA 35-2020 Quality of learning environments for students in healthcare professions - Requirements for healthcare education providers in care settings
ISO 19465:2017 Traditional Chinese medicine - Categories of traditional Chinese medicine (TCM) clinical terminological systems
ISO/TS 22990:2019 Traditional Chinese medicine — Categories of clinical terminological system to support the integration of clinical terms from traditional Chinese medicine and Western medicine
ISO 10993-18:2020/Amd.1:2022 Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
ISO/DTS 23824:2024 Medical laboratories - Guidance on application of ISO 15189 in anatomic pathology
ISO/TS 23824:2024 Medical laboratories — Guidance on application of ISO 15189 in anatomic pathology
ISO 18666:2015 Traditional Chinese medicine - General requirements of moxibustion devices
ISO/TS 17948:2014 Health informatics - Traditional Chinese medicine literature metadata
ISO/TS 16277-1:2015 Health informatics - Categorial structures of clinical findings in traditional medicine - Part 1: Traditional Chinese, Japanese and Korean medicine
ISO 18665:2015 Traditional Chinese medicine - Herbal decoction apparatus
ISO 10993-18:2020 Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process
ISO/IWA 35:2020 Quality of learning environments for students in healthcare professions - Requirements for healthcare education providers in care settings
ISO/TR 24291:2021 Health informatics - Applications of machine learning technologies in imaging and other medical applications
ISO/TS 17938:2014 Health informatics - Semantic network framework of traditional Chinese medicine language system
ISO/TS 18790-1:2015 Health informatics - Profiling framework and classification for Traditional Medicine informatics standards development - Part 1: Traditional Chinese Medicine
ISO/TR 12296:2012 Ergonomics - Manual handling of people in the healthcare sector

Ente Nazionale Italiano di Unificazione

UNI EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories
UNI ENV 12537-1:1997 Medical informatics. Registration of information objects used for EDI in healthcare. The register.
UNI EN ISO 12052:2017 Health informatics - Digital imaging and communication in medicine (DICOM) including workflow and data management
UNI EN 1614:2007 Health informatics - Representation of dedicated kinds of property in laboratory medicine
UNI ENV 12017:1998 Medical Informatics - Medical Informatics Vocabulary (MIVoc)
UNI ENV 12052:1998 Medical Informatics - Medical Imaging Communication (MEDICOM)
UNI ENV 12611:1997 Medical informatics. Categorial structure of systems of concepts. Medical devices.

Gosstandart of Russia

GOST R ISO 22367-2022 Medical laboratories. Application of risk management to medical laboratories
GOST R 52960-2008 Forensic science laboratories accreditation. Guidance on the application of GOST R ISO/IEC 17025
GOST R ISO 10993.1-1999 Medical devices. Biological evaluation of medical devices. Part 1. Evaluation and testing / Note: To be replaced by GOST R ISO 10993-1 (2009).
GOST R 59921.7-2022 Artificial Intelligence systems in clinical medicine. Algorithms of medical images analysis. Test methods. General requirements
GOST R ISO 10993.13-1999 Medical devices. Biological evaluation of medical devices. Part 13. Identification and quantification of degradation products from polymeric medical devices / Note: To be replaced by GOST R ISO 10993-13 (2009).
GOST R 59921.0-2022 Artificial intelligence systems in clinical medicine. Basic principles
GOST R 59921.3-2021 Artificial intelligence systems in clinical medicine. Part 3. Change management in AI systems with lifelong learning capability
GOST R 51538-1999 Quality systems. Medical devices. Guidance on the application of GOST R 51536-99 and GOST R 51537-99
GOST R ISO 10993.9-1999 Medical devices. Biological evaluation of medical devices. Part 9. Framework for identification and quantification of potential degradation products / Note: To be replaced by GOST R ISO 10993-9 (2009).

Bureau of Indian Standards

IS 18419-2023 Saptaparna(Alstonia Scholaris (L.) R. Br.) Stem Bark For Use In Traditional Medicine -Specification
IS 18782-2024 AnjÄ«r DashtÄ« (Ficus hispida L. f.) Dried Fruit for Use in Traditional Medicine-Specification
IS 18415-2023 Eranda(Ricinus Communis L.) Root For Use In Traditional Medicine -Specification
IS 18420-2023 Brihati (Solanum Anguivi Lam.) Root For Use In Traditional Medicine -Specification
IS/ISO 10993-18-2020 Biological evaluation of medical devices Part 18: Chemical characterization of medical device materials within a risk management process
IS 18209-2023 Shirisha Albizia Lebbeck L Benth Bark For Use In Traditional Medicine - Specification
IS 18405-2023 Karchura([Curcuma Zedoaria (Christm.) Rosc.).]Rhizome For Use In Traditional Medicine - Specification

Association Francaise de Normalisation

NF S92-081*NF EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories
NF EN ISO 10637:2018 Oral Medicine - Central Suction Systems
NF EN 1614:2006 Health IT - Representation of different types of dedicated property in laboratory medicine
NF EN ISO 20749:2018 Oral Medicine - Dental Amalgam in Pre-dosed Capsules
NF S99-501-18*NF EN ISO 10993-18:2020 Biological evaluation of medical devices - Part 18 : chemical characterization of medical device materials within a risk management process
NF EN ISO 10993-18:2020 Biological evaluation of medical devices - Part 18: chemical characterization of medical device materials within a risk management process
NF EN ISO 22367:2020 Medical biology laboratories - Application of risk management to medical biology laboratories
NF EN 1642:2013 Oral medicine - Medical devices for oral medicine - Dental implants
NF E66-055*NF ISO 2541:2017 Centre drills for centre holes with radius form - Type R
NF EN ISO 12381:2019 Health Informatics - Explicit tense expressions used in healthcare
NF X35-210*NF EN ISO 12894:2001 Ergonomics of the thermal environment - Medical supervision of individuals exposed to extreme hot or cold environments

Spanish Association for Standardization (UNE)

UNE-ENV 12388:1997 MEDICAL INFORMATICS. ALGORITHM FOR DIGITAL SIGNATURE SERVICES IN HEALTH CARE.
UNE-EN 1614:2007 Health informatics - Representation of dedicated kinds of property in laboratory medicine
AENOR UNE-ENV 12537-1:1997 Medical informatics. Registration of information objects used for EDI in healthcare. Part 1: The Registry.
UNE-ENV 12967-1:1998 MEDICAL INFORMATICS. HEALTHCARE INFORMATION SYSTEM. ARCHITECTURE (HISA). PART 1: HEALTHCARE MIDDLEWARE LAYER.
UNE-ENV 12537-2:1997 MEDICAL INFORMATICS. REGISTRATION OF INFORMATION OBJECTS USED FOR EDI IN HEALTHCARE. PART 2: PROCEDURES FOR THE REGISTRATION OF INFORMATION OBJECTS USED FOR ELECTRONIC DATA INTERCHANGE (EDI) IN HEALTHCARE.
UNE-ENV 12537-1:1997 MEDICAL INFORMATICS. REGISTRATION OF INFORMATION OBJECTS USED FOR EDI IN HEALTHCARE. PART 1: THE REGISTER.
AENOR UNE-ENV 12537-2:1997 Medical informatics. Registration of information objects used for EDI in healthcare. Part 2: Procedures for the registration of information objects used for electronic data interchange (edi) in healthcare.
UNE-ENV 12017:1998 MEDICAL INFORMATICS. MEDICAL INFORMATICS VOCABULARY (MIVOC).
UNE-EN ISO 10993-18:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
UNE-ENV 12610:1998 MEDICAL INFORMATICS. MEDICINAL PRODUCT IDENTIFICATION.
UNE-ENV 1614:1996 HEALTHCARE INFORMATICS. STRUCTURE FOR NOMENCLATURE, CLASSIFICATION, AND CODING OF PROPERTIES IN CLINICAL LABORATORY SCIENCES.
AENOR UNE-EN ISO 10993-18:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
UNE-EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
UNE-ENV 12611:1998 MEDICAL INFORMATICS. CATEGORIAL STRUCTURE OF SYSTEMS OF CONCEPTS. MEDICAL DEVICES.
UNE-ENV 13609-2:2001 Health informatics - Messages for maintenance of supporting information in healthcare systems - Part 2: Updating of medical laboratory-specific information.

Swedish Institute for Standards

SS-EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
SS-EN ISO 10993-18:2020 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)

Danish Standards Foundation

DANSK DS/ISO/TS 16277-1:2015 Health informatics - Categorial structures of clinical findings in traditional medicine - Part 1: Traditional Chinese, Japanese and Korean medicine
DS/EN 1614:2007 Health informatics - Representation of dedicated kinds of property in laboratory medicine
DANSK DS/EN 1614:2006 Health informatics - Representation of dedicated kinds of property in laboratory medicine
DS/ENV 12537-1:1997 Medical informatics - Registration of information objects used for EDI in healthcare - Part 1: The Register
DANSK DS/ISO/TS 23824:2024 Medical laboratories – Guidance on application of ISO 15189 in anatomic pathology
DANSK DS/ISO/TS 18790-1:2015 Health informatics - Profiling framework and classification for Traditional Medicine informatics standards development - Part 1: Traditional Chinese Medicine
DANSK DS/ISO/TS 17948:2014 Health informatics - Traditional Chinese medicine literature metadata
DS/ISO/TR 24291:2021 Health informatics – Applications of machine learning technologies in imaging and other medical applications
DS/CEN/CR 12587:1997 Medical Informatics - Methodology for the development of healthcare messages
DS/ENV 12610:1998 Medical informatics - Medicinal product identification
DANSK DS/EN ISO 10993-18/A1:2020 Biological evaluation of medical devices – Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
DANSK DS/ISO 22367:2020 Medical laboratories – Application of risk management to medical laboratories
DS/ENV 13609-2:2000 Health informatics - Messages for maintenance of supporting information in healthcare systems - Part 2: Updating of medical laboratory-specific information
DS/ENV 12612:1997 Medical informatics - Messages for the exchange of healthcare administrative information
DS/ENV 12611:1997 Medical informatics - Categorial structure of systems of concepts - Medical devices
DANSK DS/ISO/TR 24291:2021 Health informatics – Applications of machine learning technologies in imaging and other medical applications
DANSK DS/ISO 18615:2020 Traditional Chinese medicine – General requirements of electric radial pulse tonometric devices
DANSK DS/ISO/TR 15499:2016 Biological evaluation of medical devices – Guidance on the conduct of biological evaluation within a risk management process

German Institute for Standardization

DIN EN ISO 22367 E:2019-04 Application of medical laboratory risk management in medical laboratories (draft)
DIN EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
DIN 58959-3:2014 Medical microbiology - Quality management in medical microbiology - Part 3: Requirements for request and report forms
DIN 58959-6 Beiblatt-2 E:1991-11 Medical microbiology; quality assurance methods for the production and storage of fungi as stock and working cultures in the microbiological laboratory
DIN 58959-17 E:2007-04 Medical microbiology - Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria
DIN 58959-17 E:1991-11 Medical microbiology - Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria
DIN 58959-7 Beiblatt 2:1997 Application of quality management system in medical microbiology
DIN SPEC 91315:2014-06 General requirements for plasma sources in medicine
DIN EN ISO 22367:2019-04 Draft Document - Medical laboratories - Application of risk management to medical laboratories (ISO/DIS 22367:2019); German and English version prEN ISO 22367:2019
DIN 58959-17:2011 Medical microbiology - Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria; Text in German and English
DIN EN 1614:2006-12 Health informatics - Representation of dedicated kinds of property in laboratory medicine; English version EN 1614:2006
DIN 58959-6:1997-06 Quality management in medical microbiology - Part 6: Requirements for control strains
DIN V ENV 12017:1997 Medical Informatics - Medical Informatics Vocabulary (MIVoc); English version ENV 12017:1997
DIN 58959-6 E:1991-11 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing
DIN 58959-6 E:2016-12 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing
DIN 58959-6 Beiblatt 1:2019-06 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 1: Recommended test organisms for frequently used culture media; Text in German and Eng...
DIN 58959 Beiblatt 1:1997 Overview and index of quality management systems in medical microbiology
DIN 58959-6:2019-06 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing
DIN 58959-6:2019 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing
DIN 6878-1:1998-05 Digital archiving in medical radiology - Part 1: General requirements for the archiving of images
DIN V ENV 12967-1:1998-04 Medical informatics - Healthcare Information System Architecture (HISA) - Part 1: Healthcare Middleware Layer; English version ENV 12967-1:1998
DIN EN ISO 10993-18 E:2018-09 Biological evaluation of medical devices Part 18: Chemical characterization of medical device materials during risk management (draft)
DIN 58959-6 E:2016 Draft Document - Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing
DIN 58956-2:1986-01 Medical microbiology; medical microbiological laboratories; requirements for equipment
DIN 58959-6 Supplement 2 E:2021 Draft Document – Medical microbiology – Quality management in medical microbiology – Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 2: Recommended test organisms for frequently used testing reagents, dy...
DIN EN ISO 10993-18:2021-03 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020); German version EN ISO 10993-18:2020 / Note: To be amended by DIN EN ISO 10993-18/A1 (2021-10).
DIN 58959-3:1997-06 Quality management in medical microbiology - Part 3: Requirements for request and report forms
DIN 58956-1 Beiblatt 1:1988 Medical Microbiology Risk Grouping of Microorganisms in Medical Microbiology Laboratories
DIN EN ISO 22367:2020-09 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020); German version EN ISO 22367:2020
DIN EN 1828:2002 The structure of surgical procedure categories in the medical classification and coding system
DIN V ENV 12967-1:1998 Medical informatics - Healthcare Information System Architecture (HISA) - Part 1: Healthcare Middleware Layer; English version ENV 12967-1:1998
DIN 58957-1:1986 Medical microbiology. Safety requirements for tuberculosis examination in special medical microbiology laboratories

Canadian Standards Association (CSA)

CSA Z318.6-95-1995 Commissioning of Medical Gas Systems in Health Care Facilities General Instruction No 1 R(1999)
CSA Z318.1-95-1995 Commissioning of HVAC Systems in Health Care Facilities General Instruction No 1 R(1999)
CSA Z314.23-16:2016 Chemical sterilization of reusable medical devices in healthcare settings
CSA Z314.23-2012 Sterilization by chemical agent of reusable medical devices in healthcare establishments (first edition)
CSA IEC 62366-1-15 amd1-2021 Medical devices Part 1: Application of engineering to medical devices
CSA ISO 22367:2021 Medical laboratories - Application of risk management to medical laboratories (Adopted ISO 22367:2020, first edition, 2020-02)
CSA Z318.7-95-1995 Commissioning of Communication Systems in Health Care Facilities General Instruction No 1-2 R(1999)
CSA Z318.5-95-1995 Commissioning of Electrical Equipment and Systems in Health Care Facilities General Instruction No 1 R(1999)

The Directorate General of Specifications and Metrology (DGSM)

OS GSO ISO/TS 16277-1:2017 Health informatics -- Categorical structures of clinical findings in traditional medicine -- Part 1: Traditional Chinese, Japanese and Korean medicine

GCC Standardization Organization

GSO ISO/TS 16277-1:2017 Health informatics -- Categorical structures of clinical findings in traditional medicine -- Part 1: Traditional Chinese, Japanese and Korean medicine
BH GSO ISO/TS 18790-1:2024 Health informatics — Profiling framework and classification for Traditional Medicine informatics standards development — Part 1: Traditional Chinese Medicine
GSO ISO/TS 17948:2015 Health informatics -- Traditional Chinese medicine literature metadata
GSO ASTM F665:2014 Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application
GSO ISO 18615:2022 Traditional Chinese medicine — General requirements of electric radial pulse tonometric devices
OS GSO ISO/TS 18790-1:2024 Health informatics — Profiling framework and classification for Traditional Medicine informatics standards development — Part 1: Traditional Chinese Medicine

Lithuanian Standards Office

LST EN 1614-2007 Health informatics - Representation of dedicated kinds of property in laboratory medicine
LST L ENV 13609-2-2002 Health informatics - Messages for maintenance of supporting information in healthcare systems - Part 2: Updating of medical laboratory-specific information

American National Standards Institute （ANSI)

ANSI N13.54-2008 Fetal Radiation Dose Calculations in Nuclear Medicine
ANSI/AAMI ST58-2013(2018) Application of chemical sterilization and high-level disinfection in medical institutions

American Society of Heating, Refrigerating and Air-Conditioning Engineers (ASHRAE)

ASHRAE 3770-1994 Moisture Solubility in R-123 and R-134A
ASHRAE 3701-1993 Energy Consumption of a Mixture of R-142B/ R-22/R-12 in a Domestic Refrigerator/Freezer
ASHRAE 4299-1999 Local Heat Transfer Coefficients During Condensation of R-22 and R-32/R-125 Mixtures (The Full Test of This Paper can be Found in the International Journal of Heating@ Ventilating@ Air-Conditioning and Refrigerating Research@ Volume 5@ Number1@ January 19
ASHRAE 4313-1999 Comparision of R-22@ R-134a@ R-410a@ and R-407c Condensation Performance in Smooth and Enhanced Tubes: Part I@ Heat Transfer
ASHRAE PH-97-9-4-1997 Performance of R-32/R-125/R-134a Mixtures in Systems with Accumulators or Flooded Evaporators
ASHRAE 4314-1999 Comparision of R-22@ R-134a@ R-410a@ and R-407c Condensation Performance in Smooth and Enhanced Tubes: Part II@ Pressure Drop
ASHRAE 97-1999 Sealed Glass Tube Method to Test the Chemical Stability of Material for Use within Refrigerant Systems R(2003)
ASHRAE 4348-2000 Condensation of R-410A in a Rectangular Channel (The Full Text of This Paper Can Be Found in the International Journal of Heating@ Ventilating@ Air-Conditioning and Refrigerating Research@ Volume 5@ Number 2@ April 1999@ pp. 97-122)

Standards Norway

NS-EN 1614:2006 Health informatics — Representation of dedicated kinds of property in laboratory medicine
NS-EN ISO 10993-18:2020 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)

Association of German Mechanical Engineers

VDI 5701-2016 Biomaterials in medicine - classification@requirements and applications

Kingdom of Bahrain Testing and Metrology Directorate

BH GSO ISO/TS 17948:2017 Health informatics -- Traditional Chinese medicine literature metadata
BH GSO ASTM F665:2015 Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application
BH GSO ISO 18615:2023 Traditional Chinese medicine — General requirements of electric radial pulse tonometric devices

Association for the Advancement of Medical Instrumentation

AAMI ST58:2024 Chemical sterilization and high-level disinfection in health care facilities

Society of Automotive Engineers (SAE)

SAE AMS2750D-2005 (R) Pyrometry
SAE J2845_202111 (R) R-12 (CFC-12), R-134a (HFC-134a), R-1234yf (HFO-1234yf), R-744, and R-152a (HFC-152a), Technician Training for Service and Containment of Refrigerants Used in Mobile A/C Systems

IT-UNI

UNI EN ISO 10993-18:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process

CN-STDBOOK

图书 3-9704 2018-2019 Collection of Group Standards of the Chinese Geriatrics Society

American Society for Testing and Materials (ASTM)

ASTM F2900-11 Standard Guide for Characterization of Hydrogels used in Regenerative Medicine
ASTM F665-09(2024) Standard Classification for Vinyl Chloride Plastics Used in Biomedical Application
ASTM E1647-16 Standard Practice for Determining Contrast Sensitivity in Radiology

US-MSFC

MSFC NASA MPR 1810.1 REV I-2008 MSFC OCCUPATIONAL MEDICINE

US-CLSI

CLSI C51-A-2012 Expression of Measurement Uncertainty in Laboratory Medicine; Approved Guideline

SCC

ASQ TR1-2012 Best quality practices for biomedical research in drug development

CH-SNV

SN EN ISO 10993-18:2020 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)

AT-ON

OENORM EN ISO 10993-18:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)

PL-PKN

PN-EN ISO 10993-18-2020-11 E Biological evaluation of medical devices -- Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)

RO-ASRO

STAS 808/10-1978 PRIMARY BATTERIES BATTERIES 3R 20, 3 R20-3, 15 R 20, 40 R 12, 00 R 12, 80 R12, R 50, R 61, R 73, S 3-4 Electrical characteristics and dimcnsions

Standard Association of Australia （SAA）

AS ISO 22367:2021 Medical laboratories — Application of risk management to medical laboratories

VE-FONDONORMA

NORVEN 477-1974 Venezuelan National Standards on Medical Preventive Measures in Cases of Chlorine Poisoning

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