Quality management requirements for imported components

Quality management requirements for imported components, Total:292 items.

The international standard classification for "Quality management requirements for imported components" includes: Aerospace electric equipment and systems , Aircraft and space vehicles in general , Quality management and quality assurance , IT applications in office work , Information technology (IT) in general , Medical equipment in general .

The Chinese standard classification for "Quality management requirements for imported components" includes: Electronic components , Standardization and quality management , Basic standards and general methods , Standardization and Quality Management , Data element representing method , Medical apparatus and devices in general .

Professional Standard - Aerospace

QJ 3065.3-1998 Management Requirements for Device Manufacturing and Acceptance
QJ 3058-1998 Management Requirements for Device Evaluation
QJ 3065.4-1998 Management Requirements for Device Screening and Re-Inspection
QJ 2671-1994 Quality Management Requirements for Imported Electronic Devices
QJ 10003-2008 Screening Guide for Imported Components
QJ 3057-1998 Assurance Requirements for Aerospace Electrical, Electronic and ElectroMechanical (EEE) Devices
QJ 3152-2002 Management Requirements for New Electronic Components of Aerospace Application
QJ 3179-2003 Managerial requirements for destructive physical analysis of components
QJ 2145-1991 Regulations on Quality and Reliability Management of Electronic Components
QJ 9000A-2003 Quality management systems-Requirements
QJ 3065.1-1998 Selection and Application Management Requirements for Components?
QJ 3065.2-1998 Management Requirements for Electronic Device Procurement
QJ 9000-1998 Quality management and quality assurance requirements for the aerospace industry
QJ 3065.5-1998 Management Requirements for Device Failure Analysis

Professional Standard - Aviation

HB 9100-2023 Requirements for aviation quality management systems
HB 7679-2000 General Requirements for Management of Imported Standard Part
HB 9100-2003 Requirements for aviation quality management systems
HB 9100-2012 Requirements for aviation quality management systems
HB 7291-1996 Management Requirements for Quality of Aadvanced Research

Military Standard of the People's Republic of China-General Armament Department

GJB 1452A-2004 Quality management requirements of large scale test
GJB 3404-1998 Electronic component selection and management requirements
GJB 9001B-2009 Quality management systems requirements
GJB/Z 9001A-2001 Quality management systems - Requirements
GJB 1452-1992 Large-scale test quality management requirements
GJB 9001C-2017 Quality management systems requirements
GJB 9001A-2001 Quality management system requirements

Professional Standard - Commodity Inspection

SN/T 4315-2015 Technical requirement for the inspection of import and export electrical accessories - Export travel adaptor
SN/T 2999-2011 Requirements on Import Crude Oil Quality Evaluation
SN/T 3108-2012 Quality evaluation requirements of asphalts for import
SN/T 2790-2011 Requirements on Quality Evaluation of Import Gasoline for Motor Vehicles
SN/T 4023-2013 Quality evaluation requirement for import and export steam coal
SN/T 5048-2018 Quality and Safety Management Guidelines for Import and Export Textile Suppliers

Fujian Provincial Standard of the People's Republic of China

DB35/T 1776-2018 Technical Requirements for Quality Traceability of Imported and Exported Commodities

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

GB/T 42061-2022 Medical devices—Quality management systems—Requirements for regulatory purposes
GB/T 19004.4-1994 Quality management and quality system elements-Part 4: Guidelines for quality improvement
GB/T 43260-2023 Imported cold-chain food traceability—Requirements for traceability information management
GB/T 19001-2008 Quality management systems - Requirements
GB/T 43709-2024 Asset management informationization—Requirements for data quality management
GB/T 19001-2016 Quality management systems―Requirements
GB/T 19001-2000 Quality management systems-Requirements

Shanxi Provincial Standard of the People's Republic of China

DB14/T 3291-2025 Basic requirements for medical device business quality management
DB1410/T 113-2020 Quality management requirements for tourist attractions

Taiwan Provincial Standard of the People's Republic of China

CNS 12684-4-1996 Quality Management and Quality System Elements-Part 4:Guildelines for Quality Improvement

Group Standards of the People's Republic of China

T/HZAS 6-2020 Quality management requirements for dianthus shoots
T/QGCML 4314-2024 Label printing quality management requirements
T/CZRX 0013-2024 Quality requirements for station group management system
T/CIITA 411-2023 Digital technology—Data components—the evaluation and management of the quality
T/HZAS 23-2021 Quality management requirements for bamboo shoots
T/CAS 260-2016 Quality management systems requirements -the production organization of household electrical appliances
T/JSGS 015-2023 Technical Requirements for Digital Management of Pipe and Fitting Quality for Water Supply and Drainage

Jiangsu Provincial Standard of the People's Republic of China

DB32/T 3189-2017 Quality management system requirements for technology business incubators

Professional Standard - Certification and Accreditation

RB/T 161-2017 Quality management systems.Healthcare equipment distribution services.Requirements

Professional Standard - Military and Civilian Products

WJ 2417-1997 Quality and Reliability Information Management Requirements of Ordnance Industry

Professional Standard - Medicine

YY/T 0287-2003 Medical devices - Quality management systems - Requirements for regulatory purposes
YY/T 0287-2017 Medical devices-Quality management systems- Requirements for regulatory purposes

Professional Standard - Nuclear Industry

EJ/T 9001-2014 Requirements on quality management system for nuclear industry
EJ/T 9001-2005 Requirements on quality management system for nuclear industry

International Electrotechnical Commission (IEC)

IECQ QC 080000-EN:2017 Hazardous Substance Process Management (HSPM) System Requirements
QC 001002-5-2005 IEC Quality assessment system for Electronic Components (IECQ) - Rules of procedure - Part 5: Hazardous substance process management requirements
QC 080000-2012 IEC Quality Assessment System for Electronic Components (IECQ System) - Hazardous Substance Process Management System Requirements (HSPM)
IECQ OD 3802-2022 IEC Quality Assessment System for Electronic Components (IECQ System) - Quality system requirements for manufacturers seeking IECQ LED Component Product Certificates of Conformity for Component Product(s) associated with LED lighting
IECQ OD 3802-2015 IEC Quality Assessment System for Electronic Components (IECQ System) - Quality system requirements for manufacturers seeking IECQ LED Component Product Certificates of Conformity for Component Product(s) associated with LED lighting
QC 001002-5-2008 IEC Quality assessment system for Electronic Components (IECQ Scheme) - Rules of procedure - Part 5: Hazardous substance process management requirements (IECQ HSPM)
IECQ 080000-KR:2012 KOREAN VERSION - IEC Quality Assessment System for Electronic Components (IECQ System) - Hazardous Substance Process Management System Requirements (HSPM)
IECQ 03-5-2017 IEC Quality Assessment System for Electronic Components (IECQ System) - Rules of Procedure - Part 5: IECQ HSPM Scheme - Hazardous Substance Process Management Requirements
IECQ 03-5-2018 IEC Quality Assessment System for Electronic Components (IECQ System) - Rules of Prodecure - Part 5: IECQ HSPM Scheme - Hazardous Substance Process Management Requirements
IECQ 03-5-2012 IEC Quality Assessment System for Electronic Components (IECQ System) - Rules of Procedure - Part 5: IECQ HSPM Scheme - Hazardous Substance Process Management Requirements
IECQ 03-5-2014 IEC Quality Assessment System for Electronic Components (IECQ System) - Rules of Procedure - Part 5: IECQ HSPM Scheme - Hazardous Substance Process Management Requirements
QC 001002-1-1998 IEC quality assessment system for electronic components (IECQ) - Rules of procedure - Part 1: Administration

Ente Nazionale Italiano di Unificazione

UNI ISO 9004-4:1995 Quality management and quality system elements.
UNI EN ISO 9001:2000 Quality management systems - Requirements.
UNI EN ISO 9001:2008 Quality management systems - Requirements
UNI EN ISO 9001:2015 Quality management systems - Requirements
EC 2-2017 UNI CEI EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes
UNI CEI EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes
EC 1-2012 UNI CEI EN ISO 13485:2012 Medical devices - Quality management systems - Requirements for regulatory purposes
UNI CEI EN ISO 13485:2004 Medical devices - Quality management systems - Requirements for regulatory purposes
EC 1-2011 UNI EN ISO 13485:2004 Medical devices - Quality management systems - Requirements for regulatory purposes
EC 1-2009 UNI EN ISO 9001:2008 Quality management systems - Requirements
EC 1-2016 UNI CEI EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes
UNI CEI EN ISO 13485:2021 Medical devices - Quality management systems - Requirements for regulatory purposes
EC 3-2017 UNI CEI EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes
EC 4-2018 UNI CEI EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes
UNI EN ISO 13485:2004 Medical devices - Quality management systems - Requirements for regulatory purposes
UNI EN 9125:2025 Aerospace series - Quality management systems - Non-deliverable software requirements

Standard Association of Australia （SAA）

AS 3904.4:1994 Quality management and quality system elements - Guidelines for quality improvement
AS ISO 13485:2017 Medical devices — Quality management systems — Requirements for regulatory processes
AS 3563.1:1991 Software quality management system Part 1: Requirements
AS 3904.4(INT):1993 Quality management and quality system elements, Part 4: Guidelines for quality improvement

Society of Automotive Engineers (SAE)

SAE EIASTD4899D-2025 Requirements for an Electronic Components Management Plan
SAE EIASTD4899C Requirements for an Electronic Components Management Plan
SAE EIASTD4899B Requirements for an Electronic Components Management Plan
SAE EIASTD4899C-2017 Requirements for an Electronic Components Management Plan
SAE EIASTD4899B-2015 Requirements for an Electronic Components Management Plan
SAE AS9101G-2022 Requirements for Conducting Audits of Aviation, Space, and Defense Quality Management Systems

Danish Standards Foundation

DS/IECQ 080000 (IECQ HSPM):2006 IEC Quality Assessment System for Electronic Components (IECQ) - Electrical and Electronic Components and Products Harzardous Substance Process Management System Requirements (HSPM)
DS/ISO 9004-4:1993 Quality management and quality system elements. Part 4: Guidelines for quality improvement
DS/ISO 9004-4/Cor.1:1994 Quality management and quality system elements - Part 4: Guidelines for quality improvement
DANSK DS/EN ISO 13485:2016 Medical devices – Quality management systems – Requirements for regulatory purposes
DANSK DS/EN ISO 13485/AC:2018 Medical devices – Quality management systems – Requirements for regulatory purposes
DS/EN ISO 13485:2012 Medical devices - Quality management systems - Requirements for regulatory purposes
DS/EN ISO 9001/AC:2009 Quality management systems - Requirements
DS/EN ISO 9001/AC:2010 Quality management systems - Requirements
DS/EN ISO 9001:2008 Quality management systems - Requirements
DS/EN ISO 9001:2009 Quality management systems - Requirements
DANSK DS/EN ISO 9001/AC:2010 Quality management systems - Requirements
DS/EN ISO 9001:2011 Quality management systems - Requirements
DS/EN ISO 13485:2021 Medical devices – Quality management systems – Requirements for regulatory purposes (ISO 13485:2016)
DS/EN ISO 13485/AC:2012 Medical devices - Quality management systems - Requirements for regulatory purposes - Technical Corrigendum 1
DANSK DS/EN ISO 9001:2015 Quality management systems – Requirements (ISO 9001:2015)

Korean Agency for Technology and Standards (KATS)

KS P ISO 13485:2018 Medical devices — Quality management systems — Requirements for regulatory purposes
KS P ISO 13485-2018 Medical devices — Quality management systems — Requirements for regulatory purposes
KS P ISO 13485-2023 Medical devices — Quality management systems — Requirements for regulatory purposes
KS P ISO 13485:2007 Medical devices－Quality management systems－Requirements for regulatory purposes
KS Q ISO 9001-2024 Quality management systems — Requirements
KS Q ISO 9001:2009 Quality management systems-Requirements
KS Q ISO 9001-2018 Quality management systems — Requirements
KS Q ISO 9001-2023 Quality management systems — Requirements
KS Q ISO 9001:2018 Quality management systems — Requirements
KS Q ISO 9001-2018(2023) Quality management systems — Requirements
KS Q ISO 9001:2015 Quality management systems — Requirements
KS A 9004-4-2003 Quality management and quality system elements Part 4: Guidelines for quality improvement
KS A 9004-4-1999 Quality management and quality system elements Part 4：Guidelines for quality improvement

Bureau of Indian Standards

IS 15579-2005 Medical devices -Quality management systems-Requirements for regulatory purposes
IS/ISO 9004-4-1993 Quality Management and Quality System Elements - Part 4 : Guidelines for Quality Improvement
IS/ISO B9001-2000 Quality Management Systems - Requirements(BI-LINGUAL)

Canadian Standards Association (CSA)

CAN/CSA-ISO 13485:2016 Medical devices — Quality management systems — Requirements for regulatory purposes
CAN/CSA-ISO 13485:2003(R2013) Medical Devices - Quality Management Systems - Requirements for Regulatory Purposes
CAN/CSA-ISO 13485:2003(C2013) Medical devices - Quality management systems - Requirements for regulatory purposes
CAN/CSA-ISO 9001-2000(C2005) Quality management systems - Requirements
CAN/CSA-ISO 9001-2016(R2020) Quality management system requirements
CAN/CSA-ISO 9001:2008(R2014) Quality Management Systems - Requirements
CAN/CSA-ISO 9001-2000(R2005) Quality Management Systems - Requirements
CAN/CSA-ISO 9001:2008(C2014) Quality Management Systems - Requirements
CAN/CSA-ISO 9004-4-1994(R2001) Quality management and quality system elements - Part 4: Guidelines for quality improvement
CAN/CSA-ISO 13485:2003 Medical devices - Quality management systems - Requirements for regulatory purposes (Second Edition)
CSA ISO 13485-03-CAN/CSA:2003 Medical devices - Quality management systems - Requirements for regulatory purposes Second Edition
CSA ISO 9001-00-CAN/CSA:2000 Quality Management Systems - Requirements Third Edition; ISO 9001: 2000; Supersedes ISO 9001-94-CAN/CSA, ISO 9002-94-CAN/CSA and ISO 9003-94-CAN/CSA
CSA ISO 9001-08-CAN/CSA:2008 Quality Management Systems Fourth Edition Requirements

Association Francaise de Normalisation

NF S99-101*NF EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes
NF EN ISO 13485/A11:2021 Medical devices - Quality management systems - Requirements for regulatory purposes
NF EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes
NF S99-101/A11*NF EN ISO 13485/A11:2021 Medical devices - Quality management systems - Requirements for regulatory purposes
NF S99-101:2012 Medical devices - Quality management systems - Requirements for regulatory purposes
NF EN ISO 9001:2015 Quality management systems - Requirements
NF X50-131:2008 Quality management systems - Requirements.
NF X50-131*NF EN ISO 9001:2015 Quality management systems - Requirements
NF EN 9125:2025 Aerospace series - Quality management systems - Non-deliverable software requirements

GCC Standardization Organization

GSO ISO 13485:2016 Medical devices -- Quality management systems -- Requirements for regulatory purposes
GSO ISO 9001:2022 Quality management systems — Requirements

American National Standards Institute （ANSI)

ANSI/AAMI/ISO 13485:2016(2019) Medical devices—Quality management systems— Requirements for regulatory purposes
ANSI/ISO/ASQ Q9004:2009 Quality Management Systems - Requirements
ANSI/ISO/ASQ 9001:2008 Quality management systems - Requirements

Gosstandart of Russia

GOST 24297-1987 Input inspection of products. General
GOST R ISO 9001-2015 Quality management systems. Requirements
GOST R ISO 9001-2008 Quality management systems. Requirements
GOST ISO 9001-2011 Quality management systems. Requirements
GOST ISO 13485-2017 Medical devices. Quality management systems. Requirements for regulatory purposes
GOST R 53624-2009 Information technology. Software.Quality management systems. Requirements
GOST ISO 13485-2011 Medical devices. Quality management systems. System requirements for regulatory purposes
GOST R 54536-2011(2020) Quality management systems. Cross-sectoral requirements
GOST R 56577-2015 Quality management systems for authorities. Requirements
GOST R 54536-2011 Quality management systems. Cross-sectoral requirements

The Directorate General of Specifications and Metrology (DGSM)

OS GSO ISO 13485:2016 Medical devices -- Quality management systems -- Requirements for regulatory purposes

Spanish Association for Standardization (UNE)

UNE-EN ISO 13485:2018/A11:2022 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
UNE-EN ISO 13485:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016). (Consolidated version)
UNE-EN ISO 9001:2015 Quality management systems - Requirements (ISO 9001:2015)
AENOR UNE-EN ISO 13485/AC:2016 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
AENOR UNE 66904-4:1995 QUALITY MANAGEMENT AND ELEMENTS OF THE QUALITY SYSTEM. PART 4: GUIDELINES FOR QUALITY IMPROVEMENT.
UNE-EN ISO 13485:2004 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)
UNE-EN ISO 9001:2008 Quality management systems - Requirements (ISO 9001:2008)
UNE-EN ISO 9001:2000 Quality management systems. Requirements. (ISO 9001:2000)

Kingdom of Bahrain Testing and Metrology Directorate

BH GSO ISO 13485:2017 Medical devices -- Quality management systems -- Requirements for regulatory purposes
BH GSO ISO 9001:2023 Quality management systems — Requirements

Comitato Elettrotecnico Italiano

CEI UNI EN/ISO 13485:2017 Medical devices - Quality management systems - Requirements for regulatory purposes

American Society of Quality Control （ASQC)

ASQ Q9004-2-1991 Quality Management and Quality System Elements - Guidelines for Services
ASQ Q9004-4-1993 Quality Management and Quality System Elements - Guidelines for Quality Improvement
ASQ Q9001-2008 Quality management systems - Requirements (T860E)
ASQ Q9001-2000 Quality Management Systems - Requirements
ASQ/ISO Q9001:2015 Quality management systems -- Requirements
ASQ/ISO Q9001-2008 Quality management systems -- Requirements
ASQ Q2-1991 Quality Management and Quality System Elements for Laboratories - Guidelines T48
ASQ 9001-2015 Quality management systems - Requirements (T1040)
ASQ Q9004-1-1994 Quality Management and Quality System Elements - Guidelines; Supersedes Q94-1987
ASQ Q9004-3-1993 Quality Management and Quality System Elements - Guidelines for Processed Materials

South African Bureau of Standard

SANS 13485:2004 Medical devices - Quality management systems - Requirements for regulatory purposes
SANS 9001:2008 Quality management systems - Requirements
SANS 9001:2000 Quality management systems - Requirements

Thai Industrial Standards Institute (TISI)

TIS 13485-2004 Medical devices.quality management systems.requirements for regulatory purposes
TIS 9001-2009 Quality management systems.requirements

International Organization for Standardization (ISO)

ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes
ISO 13485:2003 Medical devices - Quality management systems - Requirements for regulatory purposes
ISO 9001:2015/Amd.1:2024 Quality management systems. Requirements
ISO 9001:2008 Quality management systems - Requirements
ISO 9001:2015 Quality management systems - Requirements
ISO 9001:2008[F] Quality management systems - Requirements [Standard in French]
ISO 9001:2000 Quality management systems - Requirements
ISO 9004-4:1993 Quality management and quality system elements - Part 4: guidelines for quality improvement
ISO 9004-4:1993/Cor 1:1994 Quality management and quality system elements - Part 4: Guidelines for quality improvement; Technical Corrigendum 1
ISO 9001:2015[F] Quality management systems - Requirements [French version]
ISO 13485:2016 Plus Redline Medical devices - Quality management systems - Requirements for regulatory purposes (includes Redline Version)

Japanese Industrial Standards Committee (JISC)

JIS Q 13485:2005 Medical devices -- Quality management systems -- Requirements for regulatory purposes
JIS Q 9001:2015 Quality management systems -- Requirements
JIS Q 9001:2008 Quality management systems -- Requirements
JIS Q 13485:2018 Medical devices -- Quality management systems -- Requirements for regulatory purposes
JIS Q 9001:2000 Quality management systems -- Requirements
JIS Q 9001 ERRATUM 1:2001 Quality management systems -- Requirements (Erratum 1)

National Standardisation Body (ASRO)

STAS 8002-1972 electric HeatinG elements IN METAL TUBES General technical requirements for quality

American Nuclear Society (ANS)

ANS 9001-2015 Quality management systems - Requirements
9001-2015 Quality management systems - Requirements

British Standards Institution (BSI)

BS EN ISO 9001:2000 Quality management systems - Requirements
BS EN ISO 9001:2015 Quality management systems. Requirements
BS EN ISO 9001:2008 Quality management systems - Requirements
BS EN ISO 9001:2015+A1:2024 Quality management systems. Requirements
24/30466228 DC BS EN ISO 10012 Quality management - Requirements for measurement management systems
BS EN ISO 13485:2012 Medical devices. Quality management systems. Requirements for regulatory purposes
BS EN ISO 13485:2003 Medical devices - Quality management systems - Requirements for regulatory purposes
07/30135834 DC BS ISO 9001. Quality management systems. Requirements
BS CECC 00806:1997 Harmonized system of quality assessment for electronic components - Guide to total quality management (TQM) for CECC approved organizations

German Institute for Standardization

DIN EN ISO 9001:2015-11 Quality management systems - Requirements (ISO 9001:2015); German and English version EN ISO 9001:2015
DIN SPEC 1115 DIN ISO TS 16949:2010-11 Quality management system requirements
DIN EN ISO 9001 2000-12 ger Quality management system requirements
DIN EN ISO 9001:1994 Quality management systems - Requirements
DIN EN ISO 9001:2000 Quality management systems - Requirements (ISO 9001:2000); Trilingual version EN ISO 9001:2000
DIN EN ISO 9001-2000 scan рус DIN EN ISO 9001-2000 scan рус
DIN EN ISO 13485 E:2014-04 Medical device quality management system regulatory requirements (draft)
DIN EN ISO 13485 E:2015-05 Medical device quality management system regulatory requirements (draft)
DIN EN ISO 13485 E:2015 Draft Document - Medical devices - Quality management systems - Requirements for regulatory purposes (ISO/DIS 13485:2015); German and English version prEN ISO 13485:2015
DIN EN ISO 13485/A1:2019 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German and English version EN ISO 13485:2016/prA1:2019
DIN EN ISO 13485:2021-12 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016); German version EN ISO 13485:2016 + AC:2018 + A11:2021
DIN EN 9101:2023-04 Aerospace series - Quality Management Systems - Requirements for conducting audits of aviation, space, and defence quality management systems; German version ASD-STAN prEN 9101:2022 / Note: Date of issue 2023-03-10*Intended as replacement for DIN EN 91...
DIN EN 9101:2024-03 Aerospace series - Quality management systems - Requirements for conducting audits of aviation, space, and defence quality management systems; German and English version EN 9101:2023
DIN ISO 13485 E:2002-05 Quality Management System Requirements for Medical Devices for Regulatory Purposes
DIN EN ISO 9001 E:2007-10 Quality management system requirements (draft)
DIN EN ISO 9001 E:1999-05 Quality management system requirements (draft)
DIN EN ISO 9001 E:2000-01 Quality management system requirements (draft)
DIN EN ISO 9001 E:2014-08 Quality management system requirements (draft)
DIN EN ISO 9001 E:1998-09 Quality management system requirements (draft)
DIN EN ISO 13485 2016 08 Requirements for medical device quality management systems for regulatory purposes
DIN EN 9101 E:2015-04 Aerospace series - Quality Management Systems - Requirements for conducting audits of aviation, space, and defence quality management systems
DIN CEN CLC ISO IEC TS 17021-3 DIN SPEC 55304-3:2016-12 Conformity assessment - Requirements for bodies providing audit and certification of management systems - Part 3: Competence requirements for auditing and certification of quality management systems
DIN EN ISO 13485:2003 Medical devices quality management systems requirements for regulatory purposes
DIN EN 9101 E:2021-10 Aerospace series - Quality Management Systems - Requirements for conducting audits of aviation, space, and defence quality management systems
DIN EN 9101 E:2017-03 Aerospace series - Quality Management Systems - Requirements for conducting audits of aviation, space, and defence quality management systems
DIN EN 45012:1998 General requirements for bodies operating assessment and certification/registration of quality systems (ISO/IEC Guide 62 : 1996)
DIN 58959-1:1997-06 Quality management in medical microbiology - Part 1: Requirements for the QM system
DIN EN ISO 10012 E:2024-11 Draft Document - Quality management - Requirements for measurement management systems (ISO/DIS 10012:2024); German and English version prEN ISO 10012:2024
DIN EN ISO 9001-9004:2000 Quality Management System Requirements (ISO 9001:2000)

European Committee for Standardization (CEN)

EN ISO 9001:2000 Quality Management Systems - Requirements Supersedes EN ISO 9002:1994 and EN ISO 9003:1994; ISO 9001:2000
EN ISO 9001:1994 Quality Systems Model for Quality Assurance in Design, Development, Production, Installation and Servicing (ISO 9001 : 1994) (Supersedes EN 29001 : 1987)
EN ISO 9001:2008 Quality management systems - Requirements
EN ISO 13485:2012 Medical devices - Quality management systems - Requirements for regulatory purposes - Technical Corrigendum 1 (Incorporating corrigendum July 2012)
EN ISO 13485:2000 Quality Systems - Medical Devices - Particular Requirements for the Application of EN ISO 9001 Revision of EN 46001:1996; Identical to ISO 13485:1996
EN ISO 13485:2016/A11:2021 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
EN ISO 13485:2016/AC:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
EN 9101:2023 Aerospace series - Quality management systems - Requirements for conducting audits of aviation, space, and defence quality management Systems
prEN 9101-2021 Requirements for Conducting Audits of Aviation, Space, and Defence Quality Management Systems
EN ISO 9001:2015 Quality management systems - Requirements (ISO 9001:2015)

Australian/New Zealand Standard (AU-AS/NZS)

AS/NZS ISO 9001:2000 Quality management systems - Requirements
AS/NZS ISO 9001(INT):2000 Quality management systems - Requirements
AS/NZS ISO 9001:2016 Quality management systems - Requirements
AS/NZS ISO 9001:2008 Quality management systems - Requirements
AS/NZS ISO 9001(SP):2000 Quality management systems - Requirements (Special edition)

Institute of Electrical and Electronics Engineers (IEEE)

IEEE Std 1298-1992 Software Quality Management System Part 1: Requirements

The Standards, Productivity and Innovation Board

SS ISO 9001:2008 Quality management systems - Requirements

Associação Brasileira de Normas Técnicas

ABNT NBR ISO 9001-2015 Quality management system requirements

Det Norske Veritas (DNV)

DNVGL-RP-B202-2017 Steel forgings for subsea applications - quality management requirements

(U.S.) Joint Electron Device Engineering Council Soild State Technology Association

JEDEC JESD671B-2012 Component Quality Problem Analysis and Corrective Action Requirements (Including Administrative Quality Problems)

Standards Norway

NS-ISO 9004-4:1993 Quality management and quality system elements — Part 4: Guidelines for quality improvement
NS-EN ISO 13485:2016 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
NS-EN ISO 13485:2012 Medical devices — Quality management systems — Requirements for regulatory purposes (ISO 13485:2003)
NS-EN ISO 13485:2016+AC:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
NS-EN ISO 13485:2003 Medical devices — Quality management systems — Requirements for regulatory purposes (ISO 13485:2003)
NS-EN ISO 13485:2016+AC:2016 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
NS-EN ISO 9001:2000 Quality management systems — Requirements (ISO 9001:2000)
NS-EN ISO 9001:2015 Quality management systems - Requirements (ISO 9001:2015)
NS-EN ISO 9001:2008 Quality management systems — Requirements (ISO 9001:2008)

Swedish Institute for Standards

SS-EN ISO 13485:2016/AC:2018 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
SIS 83 41 03-1964 Wooden storage units. Quality requirements
SS-EN ISO 9001:2015 Quality management systems - Requirements (ISO 9001:2015)
SS-EN ISO 9001:2000 Quality management systems - Requirements (ISO 9001:2000)

Association for the Advancement of Medical Instrumentation

AAMI/ISO 13485:2003(R2009) Medical Devices - Quality Management Systems - Requirements for Regulatory Purposes
AAMI/ISO 13485:2016(R2019) Medical devices - Quality management systems - Requirements for regulatory purposes
AAMI practical guide ISO 13485-2016 Medical devices 2017 Medical devices — Quality management systems — Requirements for regulatory purposes