AQAP 169 : 1
|
NATO GUIDANCE ON THE USE OF AQAP 160 EDITION 1 |
DEFSTAN 05-95/2(1992) : 1992
|
QUALITY SYSTEM REQUIREMENTS FOR THE DEVELOPMENT, SUPPLY AND MAINTENANCE OF SOFTWARE |
BS EN 62138:2009
|
Nuclear power plants. Instrumentation and control important for safety. Software aspects for computer-based systems performing category B or C functions |
CEI EN 61131-6 : 2013
|
PROGRAMMABLE CONTROLLERS - PART 6: FUNCTIONAL SAFETY |
DEFSTAN 00-55(PT2)/2(1997) : 1997 ERRATUM 1997
|
REQUIREMENTS FOR SAFETY RELATED SOFTWARE IN DEFENCE EQUIPMENT - PART 2: GUIDANCE |
DD CEN/TS 15224:2005
|
Health services. Quality management systems. Guide for the use of EN ISO 9001:2000 |
I.S. ISO 9000-2:1994
|
QUALITY MANAGEMENT AND QUALITY ASSURANCE STANDARDS - PART 2: GENERIC GUIDELINES FOR THE APPLICATION OF ISO 9001, ISO 9002 AND ISO 9003 |
DEFSTAN 05-96/1(1994) : INTERIM
|
GUIDANCE ON QUALITY SYSTEM REQUIREMENTS FOR THE IMPLEMENTATION OF DEF STAN 05-95/ISSUE 2 |
PD 0026:2003
|
Software and systems quality framework. A guide to the use of ISO/IEC and other standards for understanding quality in software and systems |
02/647837 DC : DRAFT OCT 2002
|
PD 0026 - SOFTWARE AND SYSTEM QUALITY FRAMEWORK |
CSA ISO 10993-12 : 98(R2002)
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - SAMPLE PREPARATION AND REFERENCE MATERIALS |
CSA ISO 14971 : 2007
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
TR 9109 : 1
|
AEROSPACE SERIES - GUIDELINES FOR SOFTWARE QUALITY MANAGEMENT |
ASTM E 2239 : 2012 : R2016
|
Standard Practice for Record Keeping and Record Preservation for Lead Hazard Activities |
CSA Z17665-1 : 2009 : FR
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
I.S. CWA 14172-2:2004
|
EESSI CONFORMITY ASSESSMENT GUIDANCE - PART 2: CERTIFICATION AUTHORITY SERVICES AND PROCESSES |
DEFSTAN 00-55(PT1)/2(1997) : 1997
|
REQUIREMENTS FOR SAFETY RELATED SOFTWARE IN DEFENCE EQUIPMENT - PART 1: REQUIREMENTS |
AAMI ISO 14971 : 2007 : INC : ERR 1 : 2007
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
ASTM E 2239 : 2012
|
Standard Practice for Record Keeping and Record Preservation for Lead Hazard Activities |
I.S. CWA 14172-7:2004
|
EESSI CONFORMITY ASSESSMENT GUIDANCE - PART 7: CRYPTOGRAPHIC MODULES USED BY CERTIFICATION SERVICE PROVIDERS FOR SIGNING OPERATIONS AND KEY GENERATION SERVICES |
ISO/IEC Guide 62:1996
|
General requirements for bodies operating assessment and certification/registration of quality systems |
EN 62138 : 2009
|
NUCLEAR POWER PLANTS - INSTRUMENTATION AND CONTROL IMPORTANT FOR SAFETY - SOFTWARE ASPECTS FOR COMPUTER-BASED SYSTEMS PERFORMING CATEGORY B OR C FUNCTIONS |
CEN/TS 15224:2005
|
Health services - Quality management systems - Guide for the use of EN ISO 9001:2000 |
EN 61209:1999
|
Maritime navigation and radiocommunication equipment and systems - Integrated bridge systems (IBS) - Operational and performance requirements, methods of testing and required test results |
EN 61131-6:2012
|
Programmable controllers - Part 6: Functional safety |
EN 60936-1 : 2000 AMD 1 2002
|
MARITIME NAVIGATION AND RADIOCOMMUNICATION EQUIPMENT AND SYSTEMS - RADAR - PART 1: SHIPBORNE RADAR - PERFORMANCE REQUIREMENTS - METHODS OF TESTING AND REQUIRED TEST RESULTS |
CR 13576 : 1999
|
IMPLEMENTATION OF EN 729 ON QUALITY REQUIREMENTS FOR FUSION WELDING OF METALLIC MATERIALS |
I.S. EN 62138:2009
|
NUCLEAR POWER PLANTS - INSTRUMENTATION AND CONTROL IMPORTANT FOR SAFETY - SOFTWARE ASPECTS FOR COMPUTER-BASED SYSTEMS PERFORMING CATEGORY B OR C FUNCTIONS |
04/30090382 DC : DRAFT NOV 2004
|
ISO 13408-5 - ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 5: CLEANING IN PLACE |
BS 5724-1.4(1997) : 1997
|
MEDICAL ELECTRICAL EQUIPMENT - PART 1-4: GENERAL REQUIREMENTS FOR SAFETY - COLLATERAL STANDARD - GENERAL REQUIREMENTS FOR PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS |
BS EN 61131-6:2012
|
Programmable controllers Functional safety |
DEFSTAN 00-54(PT1)/1(1999) : 1999
|
REQUIREMENTS FOR SAFETY RELATED ELECTRONIC HARDWARE IN DEFENCE EQUIPMENT - PART 1: REQUIREMENTS |
DEFSTAN 00-54(PT2)/1(1999) : 1999
|
REQUIREMENTS FOR SAFETY RELATED ELECTRONIC HARDWARE IN DEFENCE EQUIPMENT - PART 2: GUIDANCE |
BS EN 60936-1:2000
|
Maritime navigation and radiocommunication equipment and systems. Radar Shipborne radar. Performance requirements. Methods of testing and required test results |
00/202803 DC : DRAFT JUN 2000
|
|
IEC 61506:1997
|
Industrial-process measurement and control - Documentation ofapplication software |
PD6677 : 2002 (R12)
|
IMPLEMENTATION GUIDE FOR NATO AQAP-160 INCORPORATING ALL AQAP-160 TEXT AND RELEVANT ISO TEXT |
CSA E61496.1 :2004
|
SAFETY OF MACHINERY - ELECTRO-SENSITIVE PROTECTIVE EQUIPMENT - PART 1: GENERAL REQUIREMENTS AND TESTS |
AAMI TIR32 : 2004 : R2016
|
MEDICAL DEVICE SOFTWARE RISK MANAGEMENT |
04/30090379 DC : DRAFT MAR 2004
|
BS ISO 13408-4 - ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 4: CLEAN-IN-PLACE TECHNOLOGIES |
04/30048205 DC : DRAFT JUL 2004
|
BS EN ISO 17665 - STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
04/19985217 DC : DRAFT NOV 2004
|
ISO 19903 - PETROLEUM AND NATURAL GAS INDUSTRIES - FIXED CONCRETE OFFSHORE STRUCTURES |
AAMI ISO 17665-1 : 2006
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
BS EN 60872-3:2001
|
Maritime navigation and radiocommunication equipment and systems. Radar plotting aids Electronic plotting aid (EPA). Performance requirements. Methods of testing and required test results |
CEI EN 50155 : 2008
|
RAILWAY APPLICATIONS - ELECTRONIC EQUIPMENT USED ON ROLLING STOCK |
CEI UNI EN 45510-8-1 : 2000
|
GUIDE FOR PROCUREMENT OF POWER STATION EQUIPMENT - PART 8-1: CONTROL AND INSTRUMENTATION |
ASTM E 2066 : 2000
|
Standard Guide for Validation of Laboratory Information Management Systems |
ASTM E 1884 : 1997
|
Standard Guide for General Requirements for Bodies Operating Assessment and Certification/Registration of Quality Systems (Withdrawn 2004) |
ISO 14971:2007
|
Medical devices Application of risk management to medical devices |
CEI UNI EN ISO 14971 : 2013
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
I.S. EN ISO 14971:2012
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007, CORRECTED VERSION 2007-10-01) |
DIN EN ISO 17665-1:2006-11
|
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) |
DIN EN ISO 14971:2013-04
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007) |
I.S. EN ISO 10007:1997
|
QUALITY MANAGEMENT - GUIDELINES FOR CONFIGURATION MANAGEMENT |
ASME B16.5 : 2017
|
PIPE FLANGES AND FLANGED FITTINGS: NPS 1/2 THROUGH NPS 24 METRIC/INCH STANDARD |
BS 3598:1998
|
Fissile materials. Criticality safety in handling and processing. Recommendations |
CSA ISO/IEC 90003 : 2004
|
SOFTWARE ENGINEERING - GUIDELINES FOR THE APPLICATION OF ISO 9001:2000 TO COMPUTER SOFTWARE |
04/30040790 DC : DRAFT MARCH 2004
|
ISO/IEC DTR 15443-2 - INFORMATION TECHNOLOGY - SECURITY TECHNIQUES - A FRAMEWORK FOR IT SECURITY ASSURANCE - PART 2 - ASSURANCE METHODS |
I.S. EN ISO 17665-1:2006
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
03/315684 DC : DRAFT SEP 2003
|
ISO 10019 - GUIDELINES FOR THE SELECTION OF QUALITY MANAGEMENT SYSTEM CONSULTANTS AND USE OF THEIR SERVICES |
AQAP 160 : 1
|
NATO INTEGRATED QUALITY REQUIREMENTS FOR SOFTWARE THROUGHOUT THE LIFE CYCLE |
ISO 9000-1:1994
|
Quality management and quality assurance standards — Part 1: Guidelines for selection and use |
CSA CEI/IEC 300.2 : 0
|
DEPENDABILITY MANAGEMENT - PART 2: DEPENDABILITY PROGRAMME ELEMENTS AND TASKS |
DEFSTAN 05-95/3(1995) : 1995
|
QUALITY SYSTEM REQUIREMENTS FOR THE DESIGN, DEVELOPMENT, SUPPLY AND MAINTENANCE OF SOFTWARE |
BS EN 60601-1-4:1997
|
Medical electrical equipment. General requirements for safety Collateral standard. General requirements for programmable electrical medical systems |
BS ISO/IEC 21827:2008
|
Information technology. Security techniques. Systems security engineering. Capability maturity model (SSE- CMM) |
02/706744 DC : DRAFT MAY 2002
|
ISO/DIS 8178-1 - RECIPROCATING INTERNAL COMBUSTION ENGINES - EXHAUST EMISSION MEASUREMENT - PART 1: TEST-BED MEASUREMENT OF GASEOUS AND PARTICULATE EXHAUST EMISSIONS |
CSA E61496.1 : 2004 : R2013
|
SAFETY OF MACHINERY - ELECTRO-SENSITIVE PROTECTIVE EQUIPMENT - PART 1: GENERAL REQUIREMENTS AND TESTS |
BS ISO/IEC TR 13233:1995
|
Information technology. Interpretation of accreditation requirements in ISO/IEC Guide 25. Accreditation of information technology and telecommunications testing laboratories for software and protocol testing services |
SAE AS 9006 : 2013
|
DELIVERABLE AEROSPACE SOFTWARE SUPPLEMENT FOR AS9100A - QUALITY MANAGEMENT SYSTEMS - AEROSPACE - REQUIREMENTS FOR SOFTWARE |
CSA ISO/IEC 21827 : 2009
|
INFORMATION TECHNOLOGY - SECURITY TECHNIQUES - SYSTEMS SECURITY ENGINEERING - CAPABILITY MATURITY MODEL (SSE-CMM) |
CSA Z17665-1:09 (R2019)
|
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (Adopted ISO 17665-1:2006, first edition, 2006-08-15, with Canadian deviations) |
ANSI/AAMI ISO 17665-1:2006(R2013)
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
ASTM E 2066 : 2000 : R2007
|
Standard Guide for Validation of Laboratory Information Management Systems (Withdrawn 2015) |
DIN EN ISO 9241-11:2016-01 (Draft)
|
ERGONOMIC REQUIREMENTS FOR OFFICE WORK WITH VISUAL DISPLAY TERMINALS (VDTS) - PART 11: GUIDANCE ON USABILITY |
ISO/IEC 21827:2008
|
Information technology Security techniques Systems Security Engineering Capability Maturity Model (SSE-CMM) |
ISO 9002:1994
|
Quality systems — Model for quality assurance in production, installation and servicing |
BS EN ISO 14971:2012
|
Medical devices. Application of risk management to medical devices |
IEC 61249-2-19:2001
|
Materials for printed boards and other interconnecting structures - Part 2-19: Reinforced base materials, clad and unclad - Epoxide cross-plied linear fibreglass-reinforced laminated sheets of defined flammability (vertical burning test), copper clad |
IEC 62138:2004
|
Nuclear power plants - Instrumentation and control important for safety - Software aspects for computer-based systems performing category B or C functions |
NASA GB 8719.13 : 0
|
NASA SOFTWARE SAFETY GUIDEBOOK |
NASA-STD-8739.8A : 2020
|
SOFTWARE ASSURANCE AND SOFTWARE SAFETY STANDARD |
EN 45510-8-1:1998
|
Guide for procurement of power station equipment - Part 8-1: Control and instrumentation |
NASA STD 8739.8 : 2004
|
SOFTWARE ASSURANCE STANDARD |
BS IEC 61511-1 : 2003 AMD 15776
|
FUNCTIONAL SAFETY - SAFETY INSTRUMENTED SYSTEMS FOR THE PROCESS INDUSTRY SECTOR - PART 1: FRAMEWORK, DEFINITIONS, SYSTEM, HARDWARE AND SOFTWARE REQUIREMENTS |
CEI EN 62138 : 2011
|
NUCLEAR POWER PLANTS - INSTRUMENTATION AND CONTROL IMPORTANT FOR SAFETY - SOFTWARE ASPECTS FOR COMPUTER-BASED SYSTEMS PERFORMING CATEGORY B OR C FUNCTIONS |
BS ISO 17894:2005
|
Ships and marine technology. Computer applications. General principles for the development and use of programmable electronic systems in marine applications |
ISA 84.00.01-1 : 2004
|
FUNCTIONAL SAFETY: SAFETY INSTRUMENTED SYSTEMS FOR THE PROCESS INDUSTRY SECTOR - PART 1: FRAMEWORK, DEFINITIONS, SYSTEM, HARDWARE AND SOFTWARE REQUIREMENTS |
PREN 45001 : DRAFT 1997
|
GENERAL REQUIREMENTS FOR THE COMPETENCE OF TESTING AND CALIBRATION LABORATORIES |
03/314215 DC : DRAFT OCT 2003
|
ISO TR 14969 - MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
UNI CEI EN ISO 14971 : 2012
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
TR NWT 000179 : ISSUE 2
|
QUALITY SYSTEM GENERIC REQUIREMENTS FOR SOFTWARE |
BS EN ISO 9000-1:1994
|
Quality management and quality assurance standards Guidelines for selection and use |
AAMI TIR32 :2004
|
MEDICAL DEVICE SOFTWARE RISK MANAGEMENT |
AAMI ISO 14971 : 2007 : R2010
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
BS EN ISO 9241-11:1998
|
Ergonomic requirements for office work with visual display terminals (VDTs) Guidance on usability |
ISO 8402:1994
|
Quality management and quality assurance — Vocabulary |
CSA Z17665-1 : 2009 : R2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 1: REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
ISO 9003:1994
|
Quality systems Model for quality assurance in final inspection and test |
ISO 15161:2001
|
Guidelines on the application of ISO 9001:2000 for the food and drink industry |
EN ISO 14971:2012
|
Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) |
EN ISO 9241-11:1998
|
Ergonomic requirements for office work with visual display terminals (VDTs) - Part 11: Guidance on usability (ISO 9241-11:1998) |
ISO/IEC TR 13233:1995
|
Information technology Interpretation of accreditation requirements in ISO/IEC Guide 25 Accreditation of Information Technology and Telecommunications testing laboratories for software and protocol testing services |
ISO 17894:2005
|
Ships and marine technology Computer applications General principles for the development and use of programmable electronic systems in marine applications |
ISO 9004-1:1994
|
Quality management and quality system elements Part 1: Guidelines |
I.S. CWA 14172-6:2004
|
EESSI CONFORMITY ASSESSMENT GUIDANCE - PART 6: SIGNATURE-CREATION DEVICE SUPPORTING SIGNATURES OTHER THAN QUALIFIED |
S.R. CR 12804:1997
|
CONCEPTUAL MODEL AND TAXONOMY FOR INFORMATION SYSTEMS ENGINEERING |
I.S. CWA 14172-1:2004
|
EESSI CONFORMITY ASSESSMENT GUIDANCE - PART 1: GENERAL INTRODUCTION |
I.S. CWA 14172-8:2004
|
EESSI CONFORMITY ASSESSMENT GUIDANCE - PART 8: TIME-STAMPING AUTHORITY SERVICES AND PROCESSES |
IEC 61739:1996
|
Integrated circuits - Part 1: Procedures for manufacturing line approval and quality management |
GEIA HB 649 : 2005
|
CONFIGURATION MANAGEMENT STANDARD IMPLEMENTATION GUIDE |
BS EN ISO 15541:2001
|
Ships and marine technology. Fire resistance of hose assemblies. Requirements for the test bench |
BS EN ISO 17665-1:2006
|
Sterilization of health care products. Moist heat Requirements for the development, validation and routine control of a sterilization process for medical devices |
IEC 61131-6:2012
|
Programmable controllers - Part 6: Functional safety |
00/565497 DC : DRAFT DEC 2000
|
BS IEC 60601-1 MEDICAL ELECTRICAL EQUIPMENT - PART 1: GENERAL REQUIREMENTS FOR SAFETY AND ESSENTIAL PERFORMANCE |
ISO 17665-1:2006
|
Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices |
BS EN 45510-8-1:1998
|
Guide for the procurement of power station equipment Control and instrumentation |
BS EN 45012:1998
|
General requirements for bodies operating assessment and certification/registration of quality systems |
EN ISO 10007 : 1996
|
QUALITY MANAGEMENT - GUIDELINES FOR CONFIGURATION MANAGEMENT |
EN ISO 9000-1 : 1994
|
QUALITY MANAGEMENT AND QUALITY ASSURANCE STANDARDS - PART 1: GUIDELINES FOR SELECTION AND USE (ISO 9000-1:1994) |
EN ISO 17665-1 : 2006
|
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006) |
CSA ISO/IEC 90003 : 2004 : R2014
|
SOFTWARE ENGINEERING - GUIDELINES FOR THE APPLICATION OF ISO 9001:2000 TO COMPUTER SOFTWARE |
12/30264224 DC : 0
|
BS EN 61511-1 ED.2 - FUNCTIONAL SAFETY - SAFETY INSTRUMENTED SYSTEMS FOR THE PROCESS INDUSTRY SECTOR - NORMATIVE - PART 1: FRAMEWORK, DEFINITIONS, SYSTEM, HARDWARE AND SOFTWARE REQUIREMENTS |
BS ISO 15161:2001
|
Guidelines on the application of ISO 9001:2000 for the food and drink industry |
BS IEC 60300-3.6 : 1997
|
DEPENDABILITY MANAGEMENT - APPLICATION GUIDE - SOFTWARE ASPECTS OF DEPENDABILITY |
I.S. EN 45012:1998
|
GENERAL REQUIREMENTS FOR BODIES OPERATING ASSESSMENT AND CERTIFICATION/REGISTRATION OF QUALITY SYSTEMS |
DEFSTAN 05-95/1(1991) : INTERIM
|
QUALITY SYSTEM REQUIREMENTS FOR THE DEVELOPMENT, SUPPLY AND MAINTENANCE OF SOFTWARE |
BS IEC 62138 : 2004
|
NUCLEAR POWER PLANTS - INSTRUMENTATION AND CONTROL IMPORTANT FOR SAFETY - SOFTWARE ASPECTS FOR COMPUTER-BASED SYSTEMS PERFORMING CATEGORY B OR C FUNCTIONS |
98/402025 DC : DRAFT JAN 1998
|
BS ISO 13448-1 - ACCEPTANCE SAMPLING PROCEDURES BASED ON THE ALLOCATION-OF-PRIORITIES PRINCIPLE (APP) - PART 1: GUIDE TO THE APP APPROACH |
I.S. CEN TS 15224:2006
|
HEALTH SERVICES - QUALITY MANAGEMENT SYSTEMS - GUIDE FOR THE USE OF EN ISO 9001:2000 |
CSA ISO/IEC 21827 : 2009 : R2014
|
INFORMATION TECHNOLOGY - SECURITY TECHNIQUES - SYSTEMS SECURITY ENGINEERING - CAPABILITY MATURITY MODEL (SSE-CMM) |
97/402277 DC : DRAFT APR 1997
|
PREN 45001 - GENERAL REQUIREMENTS FOR THE COMPETENCE OF TESTING AND CALIBRATION LABORATORIES |
CSA ISO 14971 : 2007 : R2017
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
CSA ISO 14971 : 2007 : R2012
|
MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES |
I.S. EN 61131-6:2012
|
PROGRAMMABLE CONTROLLERS - PART 6: FUNCTIONAL SAFETY (IEC 61131-6:2012 (EQV)) |
I.S. EN ISO 9241-11:1998
|
ERGONOMIC REQUIREMENTS FOR OFFICE WORK WITH VISUAL DISPLAY TERMINALS (VDTS) - PART 11: GUIDANCE ON USABILITY |
I.S. EN CWA 14172-5:2004
|
EESSI CONFORMITY ASSESSMENT GUIDANCE - PART 5: SECURE SIGNATURE CREATION DEVICES |
I.S. EN ISO 9000-1:1994
|
QUALITY MANAGEMENT AND QUALITY ASSURANCE STANDARDS - PART 1: GUIDELINES FOR SELECTION AND USE |
I.S. EN ISO 9003:1994
|
QUALITY SYSTEMS - MODEL FOR QUALITY ASSURANCE IN FINAL INSPECTION AND TEST |
I.S. CWA 14172-4:2004
|
EESSI CONFORMITY ASSESSMENT GUIDANCE - PART 4: SIGNATURE CREATION APPLICATIONS AND GENERAL GUIDELINES FOR ELECTRONIC SIGNATURE VERIFICATION |
CR 12804 : 1997
|
CONCEPTUAL MODEL AND TAXONOMY FOR INFORMATION SYSTEMS ENGINEERING |
EN 45510-8-1:1998
|
GUIDE FOR PROCUREMENT OF POWER STATION EQUIPMENT - PART 8-1: CONTROL AND INSTRUMENTATION |
EN 60872-3:2001
|
Maritime navigation and radiocommunication equipment and systems - Radar plotting aids - Part 3: Electronic plotting aid (EPA) - Performance requirements - Methods of testing and required test results |
EN 60601-1-4:1996/A1:1999
|
MEDICAL ELECTRICAL EQUIPMENT - GENERAL REQUIREMENTS FOR SAFETY - COLLATERAL STANDARD: PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS |
DIN EN 45012:1990-05
|
GENERAL REQUIREMENTS FOR BODIES OPERATING ASSESSMENT AND CERTIFICATION/REGISTRATION OF QUALITY SYSTEMS |