healthcare routine

healthcare routine, Total:248 items.

The international standard classification for "healthcare routine" includes: Other standards related to sterilization and disinfection , Sterilization and disinfection , Sterilization and disinfection in general .

The Chinese standard classification for "healthcare routine" includes: Public medical equipment .

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

GB/T 19974-2018 Sterilization of health care products—General requirement for characterization of a sterilization agent and the development, validation and routine control of a sterilization process for medical devices
GB/T 19971-2015 Sterilization of health care products―Vocabulary
GB/T 20367-2006 Sterilization of health care products - Requirement for validation and routine control of moist heat sterilization in health care facilities
GB 18280-2000 Sterilization of health care products—Requirement for validation and routine control—Radiation sterilization
GB 18278-2000 Sterilization of health care products - Requirements for validation and routine control - Industrial moist heat sterilization
GB 18278.1-2015 Sterilization of health care products―Moist heat―Part 1:Requirements for the development, validation and routine control of a sterilization process for medical devices
GB 18279-2023 Sterilization of health-care products—Ethylene oxide—Requirements for the development,validation and routine control of a sterilization process for medical devices
GB 18280.1-2015 Sterilization of health care products―Radiation―Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices
GB 18279.1-2015 Sterilization of health care products―Ethylene oxide―Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices
GB/T 19974-2005 GB/T 1997 4-2005 Sterilization of health care products - General requirement for characterization of a sterilization agent and the development, validation and routine control of a sterilization proce
GB/T 19971-2005 Sterilization of health care products-Vocabulary

Shanghai Provincial Standard of the People's Republic of China

DB31/T 492-2010 Cadre health care and medical service norms

未注明发布机构

ANSI/AAMI/ISO 14937:2009(2013) Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
NFPA 99-2024 Health Care Facilities Code
ANSI/AAMI/ISO 11135:2014 Sterilization of health care products — Ethylene oxide — Requirements for development, validation and routine control of a sterilization process for medical devices
CSA ISO 20857:2019 Sterilization of health care products — Dry heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
CSA Z8002-2019 Operation and maintenance of health care facilities
CSA Z387-2019 Safe use of electrosurgical medical devices and systems in health care
DIN EN 16686 E:2014-01 Osteopathic healthcare provision
CSA Z8000-2018 Canadian healthcare facilities
DIN EN ISO 11135 E:2011-09 Requirements for the development, validation and routine control of ethylene oxide medical device sterilization processes for sterilization of healthcare products (draft)

Group Standards of the People's Republic of China

T/CACM 1560.3-2023 Technical operation specifications of Chinese medicine health care services (Non-medical)—Cupping
T/CACM 1560.10-2023 Specification for operation technologies of traditional Chinese medicine health care services (non-medical)—Fumigation and steaming
T/CAGR 013-2024 Traditional Chinese medicine therapy in sanatorium General introduction
T/CACM 1560.1-2023 Technical operation specifications of Chinese medicine health care services（non-medical）— Tuina (the traditional Chinese massage)
T/CACM 1560.2-2023 Technical operation specifications of Chinese medicine health care services（non-medical）— Guasha
T/GDNS 007-2023 Medical and Health Personal Information Protection Specifications
T/CACM 1560.4-2023 Technical operation specifications of Chinese medicine health care services (Non-medical)—Moxibustion
T/HSIPA 005-2022 Dehe Traditional Chinese Medicine Head Therapy and Health Care Technical Operation Specifications
T/CACM 1560.9-2023 Specification for operation technologies of traditional Chinese medicine health care services (non-medical)—Foot bath

Xizang Provincial Standard of the People's Republic of China

DB54/T 0200-2020 Regulations on medical care services in pension institutions
DB54/T 0216-2020 Regulations on Medical and Health Care Services of Child Welfare Institutions

国家药监局

YY/T 1464-2022 Sterilization of health care products-Low temperature steam and formaldehyde-Requirements for development,validation and routine control of a sterilization process for medical devices

International Organization for Standardization (ISO)

ISO 13683:1997 Sterilization of health care products - Requirements for validation and routine control of moist heat sterilization in health care facilities
ISO 11137:1995 Sterilization of health care products - Requirements for validation and routine control - Radiation sterilization
ISO/DIS 11135 Sterilization of health care products — Ethylene oxide — Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO 11134:1994 Sterilization of health care products; requirements for validation and routine control; industrial moist heat sterilization
ISO 11135:2014 Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO 11137:1995/Amd 1:2001 Sterilization of health care products - Requirements for validation and routine control - Radiation sterilization; Amendment 1: Selection of terms for dose setting
ISO/DIS 17665 Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO 11137:1995/Cor 1:1997 Sterilization of health care products - Requirements for validation and routine control - Radiation sterilization; Technical Corrigendum 1
ISO/FDIS 17665:2023 Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO 20857:2010 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO 25424:2018/Amd 1:2022 Sterilization of health care products — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devices — Amendment

British Standards Institution (BSI)

BS EN 16224:2012 Healthcare provision by chiropractors
BS EN 16224:2012+A1:2014 Healthcare provision by chiropractors
BS EN ISO 11137-1:2015 Sterilization of health care products. Radiation. Requirements for development, validation and routine control of a sterilization process for medical devices
BS EN ISO 11137-1:2006+A1:2013 Sterilization of health care products - Radiation - Requirements for development, validation and routine control of a sterilization process for medical devices
BS DD ENV 12443:2001 Medical informatics - Healthcare information framework (HIF)
BS ISO 7101:2023 Healthcare organization management. Management systems for quality in healthcare organizations. Requirements
BS EN ISO 11135:2014 Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices
PD CR 13644:2001 Machine readable cards. Healthcare applications. Logical organization of data on healthcare professional cards
BS DD ISO/TS 22220:2011 Health informatics. Identification of subjects of health care
BS ISO 22886:2020 Healthcare organization management. Vocabulary
BS ISO 18250-1:2018 Medical devices. Connectors for reservoir delivery systems for healthcare applications - General requirements and common test methods
24/30485888 DC BS EN ISO 11135 Sterilization of health care products - Ethylene oxide -Requirements for the development, validation and routine control of a sterilization process for medical devices
BS CWA 16642:2013 Health care services. Quality criteria for health check
DD ISO/TS 22220:2011 Health informatics. Identification of subjects of health care
BS EN ISO 17665:2024 Sterilization of health care products. Moist heat. Requirements for the development, validation and routine control of a sterilization process for medical devices
BS DD ENV 12612:1998 Medical informatics - Messages for the exchange of healthcare administrative information
DD ENV 12443:2001 Medical informatics. Healthcare information framework (HIF)
DD ENV 12443-2001 Medical informatics. Healthcare information framework (HIF)
BS ISO 5741:2023 Healthcare organization management. Pandemic response. Temporary medical facility
BS EN ISO 20857:2013 Sterilization of health care products. Dry heat. Requirements for the development, validation and routine control of a sterilization process for medical devices
DD ISO/TS 80004-7:2011 Nanotechnologies. Vocabulary. Diagnostics and therapeutics for healthcare
PD 6610:1997 Medical informatics. Methodology for the development of healthcare messages
BS DD ENV 12537-1:1998 Medical informatics - Registration of information objects used for EDI in healthcare - The register

Association Francaise de Normalisation

NF S99-802*NF EN 16224+A1:2014 Healthcare provision by chiropractors
NF S98-104*NF EN ISO 20857:2013 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
NF EN ISO 20857:2013 Sterilization of healthcare products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
NF X50-560*NF EN 17398:2020 Patient involvement in health care - Minimum requirements for person-centred care
NF X30-506:2007 Health care waste - Packaging for infectious liquid health care waste - Specifications and tests.
NF EN ISO 11135:2014 Sterilization of healthcare products - Ethylene oxide - Requirements for development, validation and routine control of a sterilization process for medical devices
NF X30-510:2010 Terminology of health care waste.
XP S98-224*XP ISO/TS 22421:2021 Sterilization of health care products - Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
NF X30-510:2003 Terminology of health care waste.
NF EN 15224:2017 Health services - Quality management systems - Application of EN ISO 9001:2015 to health care
NF S98-103-1*NF EN ISO 11137-1:2016 Sterilization of health care products - Radiation - Part 1 : requirements for development, validation and routine control of a sterilization process for medical devices
NF EN ISO 13120:2019 Health Informatics - Content Representation Syntax of Healthcare Classification Systems - Classification Marking Language (ClaML)
NF EN ISO 14937:2009 Sterilization of healthcare products - General requirements for the characterization of a sterilizing agent and for the development, validation and routine verification of a sterilization process for medical devices
NF S98-101*NF EN ISO 11135:2014 Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
NF EN 16872:2016 Health services of medical doctors with additional qualification in homeopathy - Requirements for health care services provided by medical doctors with additional qualification in homeopathy
NF EN ISO 25424/A1:2022 Sterilization of healthcare products - Formaldehyde and low temperature steam - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1

European Committee for Standardization (CEN)

EN 16686:2015 Osteopathic healthcare provision
DD ENV 12 381-1996 Health Care Informatics - Time Standards for Healthcare Specific Problems
DD ENV 12967-1-1998 Medical Informatics - Healthcare Information System Architecture (HISA) - Part 1: Healthcare Middleware Layer
DD ENV 14237-2002 Textiles in the Healthcare System
EN ISO 20857:2013 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
prEN ISO 11137-1 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11137-1:2023)
DD ENV 12443-1999 Medical informatics - Healthcare Information Framework (HIF)
EN ISO 11137-1:2006/A1:2013 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/Amd 1:2013)

National Fire Protection Association (NFPA)

NFPA FPH SECTION 13-8-2003 Healthcare Occupancies
NFPA 99H CHAPTER 14-2002 Other Health Care Facilities
NFPA 101H CHAPTERS 18&19-2006 New and Existing Health Care Occupancies

CEN - European Committee for Standardization

DD ENV 12381-1996 Health Care Informatics - Time Standards for Healthcare Specific Problems

SCC

BS DD ENV 12381:1997 Health care informatics. Time standards for healthcare specific problems
AS 2786:1985 Symbols - Health care in hospitals
DANSK DS/EN ISO 17665:2024 Sterilization of health care products – Moist heat – Requirements for the development, validation and routine control of a sterilization process for medical devices
DIN V ENV 12967-1:1998 Medical informatics - Healthcare Information System Architecture (HISA) - Part 1: Healthcare Middleware Layer; English version ENV 12967-1:1998
AAMI ST90:2017 Processing of health care products - Quality management systems for processing in health care facilities
CSA Z317.14-2017(R2022) Wayfinding for health care facilities
NS-EN 16686:2015 Osteopathic healthcare provision
AAMI/ISO 11135:2014 Sterilization of health care products - Ethylene oxide - Requirements for development, validation and routine control of a sterilization process for medical devices
DANSK DS/EN 16686:2015 Osteopathic healthcare provision
NS 3380:2018 Healthcare services — Bed sheets
NS-EN ISO 17665:2024 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)
CAN/CSA Z8001-2013(R2023) Commissioning of health care facilities
CSA Z8001-13:2013 Commissioning of health care facilities
UNE-ENV 12967-1:1998 MEDICAL INFORMATICS. HEALTHCARE INFORMATION SYSTEM. ARCHITECTURE (HISA). PART 1: HEALTHCARE MIDDLEWARE LAYER.
CSA Z318.0-1993(R2012) Commissioning of Health Care Facilities
CSA Z318.0-2005(R2012) Commissioning of Health Care Facilities
CSA Z8000-2018(R2023) Canadian health care facilities
07/30164697 DC ISO 20857. Sterilization of health care products. Dry heat. Requirements for the development, validation and routine control of an industrial sterilization process for medical devices
DANSK DS/CEN/CR 13644:2001 Machine readable cards - Healthcare applications - Logical organisation of data on healthcare professional cards
CSA Z317.10-2015(R2020) Handling of Waste Materials in Health Care Facilities and Veterinary Health Care Facilities
BS PD CR 13644:2001 Machine readable cards. Healthcare applications. Logical organization of data on healthcare professional cards
DIN EN ISO 20857 E:2012 Draft Document - Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010); German version FprEN ISO 20857:2012
DIN EN ISO 17665 E:2022 Draft Document - Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 17665:2022); German and English version prEN ISO 17665:2022
SN-CR 14301:2002 Health informatics — Framework for security protection of healthcare communication
CAN/CSA-Z317.10-2001(R2007) Handling of Waste Materials in Health Care Facilities and Veterinary Health Care Facilities
DANSK DS/CEN/CR 14301:2002 Health informatics - Framework for security protection of healthcare communication
04/30048118 DC BS EN ISO 11135. Sterilization of health care products. Ethylene oxide. Requirements for development, validation and routine control of a sterilization process for medical devices
AAMI/ISO 11135-1:2007 Sterilization of health care products - Ethylene oxide - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
DANSK DS/EN ISO 11135-1:2007 Sterilization of health care products – Ethylene oxide – Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
AAMI/ISO 14937:2000 Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
DANSK DS/ISO 22441:2022 Sterilization of health care products – Low temperature vaporized hydrogen peroxide – Requirements for the development, validation and routine control of a sterilization process for medical devices
DANSK DS/ISO 20857:2010 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
BS DD ISO/TS 22220:2009 Health informatics. Identification of subjects of health care
VDI 4075 BLATT 5-2014 Production-integrated environmental protection (PIUS) — Healthcare
CAN/CSA-Z11135-1-2009(R2014) Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
11/30244091 DC BS EN ISO 11135. Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices
VDI 4075 BLATT 5-2014 Production-integrated environmental protection (PIUS) — Healthcare
CSA DIR.003-1998 List of CSA Certified Health Care Equipment
DANSK DS/EN ISO 20857:2013 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
BS EN ISO 11137-1:2006 Sterilization of health care products. Radiation. Requirements for development, validation and routine control of a sterilization process for medical devices
CSA Z317.11-17:2017 Area measurement for health care facilities
CAN/CSA Z317.11-2017(R2022) Area Measurement for Health Care Facilities
NS-ENV 12443:1999 Medical Informatics — Healthcare Information Framework (HIF)
CAN/CSA-ISO 20857-2019 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
UNE-ENV 14237:2003 Textiles in the healthcare system.
CAN3 Z317.11-M82-1982(R1999) Area Measurement for Health Care Facilities
NS-ENV 14237:2002 Textiles in the healthcare system
SN-CWA 16642:2013 Health care services - Quality criteria for health checks
CAN/CSA Z317.11-2002(R2013) Area Measurement for Health Care Facilities
DANSK DS/EN ISO 14937:2009 Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
CAN/CSA-Z317.11-2002(R2013) Area Measurement for Health Care Facilities
DIN EN ISO 11135 E:2012 Draft Document - Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2012); German version prEN ISO 11135:2012
BS PD 6610:1997 Medical informatics. Methodology for the development of healthcare messages
SN-CR 12587:1996 Medical Informatics — Methodology for the development of healthcare messages
CSA Z387-2013(R2018) Safe use of electrosurgical medical devices and systems in health care
DANSK DS/CEN/CR 12587:1997 Medical Informatics - Methodology for the development of healthcare messages
CSA Z318.1-1995(R2001) Commissioning of HVAC Systems in Health Care Facilities
CAN/CSA-Z317.5-M89-1989 Illumination Systems in Health Care Facilities
SN/TS 6600:2020 Management systems for cleaning in the health care service
NS 3357:2024 Healthcare service - Unisex trousers
CSA Z317.5-2017(R2022) Illumination Systems in Health Care Facilities
CAN/CSA-Z386-1992 Laser Safety in Health Care Facilities
NS 3302:2021 Healthcare services - Leno woven blankets
CAN/CSA-ISO 14937-2001(R2011) Sterilization of Health Care Products - General Requirements for Characterization of a Sterilizing Agent and the Development, Validation and Routine Control of a Sterilization Process for Medical Devices
CAN 3-Z317.11-M82-1982 Measuring Areas in Medical Care Facilities
NZS PAS 8170:2005 Primary Healthcare Practice Management Systems
DIN EN ISO 11137-1 E:2023 Draft Document - Sterilization of health care products - Radiation - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11137-1:2023); German and English version prEN ISO 111...
DIN EN ISO 25424 E:2017 Draft Document - Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO/DIS 25424:2017); German and English versi...
CSA Z8002-2014(R2018) Operation and maintenance of health care facilities
CAN/CSA Z317.10-1988(R1998) Handling of Waste Materials Within Health Care Facilities
CSA Z317.5-1998(R2013) Illumination Systems in Health Care Facilities
CSA Z386-2001 Laser Safety in Health Care Facilities
SA HB 234-2012 Healthcare identifier HL7 implementation guide
NS-EN 16224:2012 Healthcare provision by chiropractors

PL-PKN

PN-EN 17398-2020-11 E Patient involvement in health care -- Minimum requirements for person-centred care

German Institute for Standardization

DIN EN 17398:2019 Patient involvement in health care - Minimum requirements for person-centred care; German and English version prEN 17398:2019
DIN EN 16686:2015-09 Osteopathic healthcare provision; German version EN 16686:2015
DIN EN ISO 17665:2024 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)
DIN EN ISO 11137-1:2020-04 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd.1:2013 + Amd.2:2018); German version EN ISO 11137-1...
DIN EN 16224:2012 Healthcare provision by chiropractors; German version EN 16224:2012
DIN EN ISO 11135:2024-04 Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135.2:2024); German and English version prEN ISO 11135:2024
DIN EN 17398:2020 Patient involvement in health care - Minimum requirements for person-centred care; German version EN 17398:2020
DIN EN ISO 11135:2023-05 Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2023); German and English version prEN ISO 11135:2023 / Note: Date o...
DIN EN 16224:2015 Healthcare provision by chiropractors; German version EN 16224:2012+A1:2014
DIN EN ISO 17665:2022-11 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 17665:2022); German and English version prEN ISO 17665:2022 / Note: Date of is...
DIN EN ISO 20857:2013-08 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010); German version EN ISO 20857:2013
DIN EN 16224:2015-03 Healthcare provision by chiropractors; German version EN 16224:2012+A1:2014
DIN V ENV 12443:2000 Medical informatics - Healthcare Information Framework (HIF); English version ENV 12443:1999
DIN EN ISO 11135:2020-04 Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018); German version EN ISO 11135:2014 + A1:2019

CH-SNV

SN EN 17398-2020 Patient involvement in health care - Minimum requirements for person-centred care

IT-UNI

UNI EN 17398-2021 Patient involvement in health care - Minimum requirements for person-centred care

Danish Standards Foundation

DS/ISO/TS 22421:2021 Sterilization of health care products – Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
DS/ENV 12443:2000 Medical Informatics - Healthcare Information Framework (HIF)
DS/EN ISO 11137-1/A1:2013 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
DS/EN ISO 11137-1:2006 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
DS/CEN/CR 13644:2001 Machine readable cards - Healthcare applications - Logical organisation of data on healthcare professional cards
DS/EN ISO 20857:2013 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
DS/EN ISO 14937:2009 Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices

Standard Association of Australia （SAA）

AS 2828:1999 Paper-based health care records
AS/NZS 2500:2020 Safe use of medical electrical equipment in health care
AS 4083:2010 Planning for emergencies—Health care facilities

AENOR

UNE-ENV 12443:2000 Medical Informatics - Healthcare Information Framework (HIF)
UNE-EN ISO 20857:2013 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010)

ES-UNE

UNE-EN 16686:2015 Osteopathic healthcare provision
UNE-EN ISO 11137-1:2015 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)

Illuminating Engineering Society of North America

IESNA HB-9 CHAPTER 16-2000 Health Care Facility Lighting
IESNA RP-29-2006 Lighting for Hospitals and Health Care Facilities

American National Standards Institute （ANSI)

ANSI/CAP SNOMED-1-2003 Healthcare Terminology Structure
ISO/DIS 11135:2023 Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
ANSI/ASTM E2084:2000 Specification for Authentication of Healthcare Information using Digital Signatures
ANSI/ASTM E2085:2001 Guide on Security Framework for Healthcare Information
ANSI/ASTM E1762:1997 Guide for Electronic Authentication of Health Care Information

Canadian Standards Association (CSA)

CSA ISO 14937-01-CAN/CSA:2001 Sterilization of Health Care Products - General Requirements for Characterization of a Sterilizing Agent and the Development, Validation and Routine Control of a Sterilization Process for Medical Devices First Edition; ISO 14937:2000
CSA Z317.10-09 UPD 1-2009 Handling of waste materials in health care facilities and veterinary health care facilities Third Edition
CSA ISO 11137-98-CAN/CSA:1998 Sterilization of Health Care Products - Requirements for Validation and Routine Control - Radiation Sterilization ISO 11137: 1995
CSA DIR.003-99 List of CSA Certified Health Care Equipment
CAN/CSA-ISO 14937:2011 Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (Second Edition)

VDI - Verein Deutscher Ingenieure

VDI 4075 Blatt 5-2012 Produktionsintegrierter Umweltschutz (PIUS) - Gesundheitswesen

Japanese Industrial Standards Committee (JISC)

JIS T 0806-1:2022 Sterilization of health care products -- Radiation -- Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices

NEMA - National Electrical Manufacturers Association

NEMA ANSI/NEMA SC 1-2019 Supplier Credentialing in Healthcare

GSO

OS GSO ISO 11137-1:2014 Sterilization of health care products -- Radiation -- Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
BH GSO ISO 11137-1:2015 Sterilization of health care products -- Radiation -- Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
GSO ISO 22441:2024 Sterilization of health care products — Low temperature vaporized hydrogen peroxide — Requirements for the development, validation and routine control of a sterilization process for medical devices
OS GSO ISO 20857:2016 Sterilization of health care products -- Dry heat -- Requirements for the development, validation and routine control of a sterilization process for medical devices
GSO ISO 20857:2016 Sterilization of health care products -- Dry heat -- Requirements for the development, validation and routine control of a sterilization process for medical devices
BH GSO ISO 20857:2017 Sterilization of health care products -- Dry heat -- Requirements for the development, validation and routine control of a sterilization process for medical devices
GSO ISO 11135:2014 Sterilization of health-care products -- Ethylene oxide -- Requirements for the development, validation and routine control of a sterilization process for medical devices
BH GSO ISO 11135:2015 Sterilization of health-care products -- Ethylene oxide -- Requirements for the development, validation and routine control of a sterilization process for medical devices

RU-GOST R

GOST R ISO 17665-1-2016 Sterilization of health care products. Moist heat. Part 1. Requirements for development, validation and routine control of a sterilization process for medical device
GOST ISO/TS 22220-2013 Health informatics. Identification of subjects of health care
GOST R ISO 14937-2012 Sterilization of health care products. General criteria for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices

KR-KS

KS P ISO 25424-2020 Sterilization of health care products — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devices

Korean Agency for Technology and Standards (KATS)

KS P ISO 25424:2020 Sterilization of health care products — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devices
KS P ISO 14937-2023 Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
KS X ISO TS 22220-2022 Health informatics — Identification of subjects of health care
KS P ISO 11137-1:2008 Sterilization of health care products－Radiation－Part 1：Requirements for development, validation and routine control of a sterilization process for medical devices

VN-TCVN

TCVN 7393-1-2009 Sterilization of health care products.Radiation.Part 1: Requirements for developement, validation and routine control of a sterilization process for medical devices.
TCVN 7392-1-2009 Sterilization of health care products.Ethylene oxide.Part 1: Requirements for developement validation and routine control of a sterilization process for medical devices.

NZ-SNZ

SAA/SNZ HB 228-2001 Guidelines for Managing Risk in Healthcare

TH-TISI

TIS 2501-2010 Textiles in the healthcare system

NZS

SAA/SNZ HB 228:2001 Guidelines for managing risk in healthcare

UNKNOWN

GB/T 18279.1-2015 Ethylene oxide for sterilization of healthcare products Part 1: Requirements for the development, validation and routine control of sterilization processes for medical devices

Institute of Electrical and Electronics Engineers (IEEE)

IEEE Std 602-1996 IEEE Recommended Practice for Electric Systems in Health Care Facilities
ANSI/IEEE Std 602-1986 IEEE Recommended Practice for Electric Systems in Health Care Facilities
NFPA (Fire) 99 Health Care Facilities Code, 2021 Edition
IEEE Std 602-2007 IEEE Recommended Practice for Electric Systems in Health Care Facilities

Lithuanian Standards Office

LST L ENV 14237-2004 Textiles in the healthcare system
LST EN ISO 14937:2010 Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009)

US-CFR-file

CFR 42-424.530-2014 Public Health. Part424:Conditions for Medicare payment. Section424.530:Denial of enrollment in the Medicare program.

American Society for Testing and Materials (ASTM)

ASTM F2407/F2407M-23 Standard Specification for Surgical Gowns Intended for Use in Healthcare Facilities
ASTM F2407/F2407M-22a Standard Specification for Surgical Gowns Intended for Use in Healthcare Facilities

IMO - International Maritime Organization

TA115E VOL 1-2000 Medical Care. Course and Compendium Volume 1
TA115E VOL 2-2000 Medical Care. Course and Compendium Volume 2