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CSA Z364.2.1 - MONITORING SYSTEMS FOR HEMODIALYSIS EQUIPMENT - THIRD EDITION Organization: CSA
Date: 2013-03-01
Description: 2) For requirements for monitoring water quality, users should consult CAN/CSA-ISO 11663, CAN/CSA-ISO 13959, and CAN/CSA-ISO 26722.
ASTM F2166 - STANDARD PRACTICES FOR MONITORING NON-CONTACT DIELECTRIC CHARACTERIZATION SYSTEMS THROUGH USE OF SPECIAL REFERENCE WAFERS Organization: ASTM
Date: 2002-01-10
Description: The procedures in this practice can be used to ascertain that the dielectric characterization system(s) meet quality control requirements such as those in an ISO 9000 quality program. This standard does not purport to address all of the safety concerns, if any, associated with its use.
NBN - CEN/TR 15592 - HEALTH SERVICES - QUALITY MANAGEMENT SYSTEMS - GUIDE FOR THE USE OF EN ISO 9004:2000 IN HEALTH SERVICES FOR PERFORMANCE IMPROVEMENT Organization: NBN
Date: 2007-05-01
Description: This International Standard provides guidelines beyond the requirements given in ISO 9001 in order to consider both the effectiveness and efficiency of a quality management system, and consequently the potential for improvement of the performance of an organization.
NBN - CEN/TR 15592 - HEALTH SERVICES - QUALITY MANAGEMENT SYSTEMS - GUIDE FOR THE USE OF EN ISO 9004:2000 IN HEALTH SERVICES FOR PERFORMANCE IMPROVEMENT Organization: NBN
Date: 2007-05-01
Description: This International Standard provides guidelines beyond the requirements given in ISO 9001 in order to consider both the effectiveness and efficiency of a quality management system, and consequently the potential for improvement of the performance of an organization.
DS/CEN/TR 15592 - HEALTH SERVICES - QUALITY MANAGEMENT SYSTEMS - GUIDE FOR THE USE OF EN ISO 9004:2000 IN HEALTH SERVICES FOR PERFORMANCE IMPROVEMENT Organization: DS
Date: 2007-06-22
Description: This International Standard provides guidelines beyond the requirements given in ISO 9001 in order to consider both the effectiveness and efficiency of a quality management system, and consequently the potential for improvement of the performance of an organization.
NPFC - DI-SESS-81921 - QUALITY AUDIT SITE VISIT REPORT (QASVR) Organization: NPFC
Date: 2013-07-10
Description: Some examples of third-party quality standards to which this DID could apply are as follows: ISO9001 (Quality Management Systems – Requirements), ISO/IEC17025 (General Requirements for the Competence of Testing and Calibration Laboratories), ANSI/ISO/ASQ Q9001 (Quality Management Systems − Requirements), and SAE AS9100 (Quality Management Systems: Aerospace Requirements).
NPFC - DI-SESS-81923 - QUALITY AUDIT FINDING AND RESPONSE RECORD (QAFRR) Organization: NPFC
Date: 2013-07-10
Description: Some examples of third-party quality standards to which this DID could apply are as follows: ISO9001 (Quality Management Systems – Requirements), ISO/IEC17025 (General Requirements for the Competence of Testing and Calibration Laboratories), ANSI/ISO/ASQ Q9001 (Quality Management Systems − Requirements), and SAE AS9100 (Quality Management Systems: Aerospace Requirements).
CEI EN 62387-1 - RADIATION PROTECTION INSTRUMENTATION - PASSIVE INTEGRATING DOSIMETRY SYSTEMS FOR ENVIRONMENTAL AND PERSONAL MONITORING PART 1: GENERAL CHARACTERISTICS AND PERFORMANCE REQUIREMENTS Organization: CEI
Date: 2012-11-01
Description: The test utilizing radiation (Clauses 13 to 15) shall be done with neutron reference radiation qualities according to the ISO 8529 series. In some countries the presence of beta dose has to be indicated by dosemeters worn on the trunk.
CENELEC - EN 62387-1 - RADIATION PROTECTION INSTRUMENTATION - PASSIVE INTEGRATING DOSIMETRY SYSTEMS FOR ENVIRONMENTAL AND PERSONAL MONITORING - PART 1: GENERAL CHARACTERISTICS AND PERFORMANCE REQUIREMENTS Organization: CENELEC
Date: 2012-02-01
Description: The test utilizing radiation (Clauses 13 to 15) shall be done with neutron reference radiation qualities according to the ISO 8529 series. In some countries the presence of beta dose has to be indicated by dosemeters worn on the trunk.
DIN EN 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 11137-1:2006, INCLUDING AMD 1:2013) Organization: DIN
Date: 2015-11-01
Description: See, for example, EN 556-1 or ANSI/AAMI ST67. This part of ISO 11137 does not specify a quality management system for the control of all stages of production of medical devices.
ISO - ISO DIS 28902-2 - AIR QUALITY - ENVIRONMENTAL METEOROLOGY - PART 2: GROUND-BASED REMOTE SENSING OF WIND BY HETERODYNE PULSED DOPPLER LIDAR Organization: ISO
Date: 2015-01-26
Description: This International Standard may be used for the following application areas:  — meteorological briefing for e.g. aviation, airport safety, marine applications, oil platforms; — wind power production, e.g. site assessment, power curve determination; — routine measurements of wind profiles at meteorological stations; — air pollution dispersion monitoring; — industrial risk management (direct data monitoring or by assimilation into micro‐scale flow models); — exchange processes (greenhouse gas emissions).
AAMI 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS—RADIATION—PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION, AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES - INCORPORATES AMENDMENT 1: 2013 Organization: AAMI
Date: 2006-01-01
Description: See, for example, EN 556-1 or ANSI/AAMI ST67. This part of ISO 11137 does not specify a quality management system for the control of all stages of production of medical devices.
CEN - EN 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 Organization: CEN
Date: 2015-06-01
Description: See, for example, EN 556-1 or ANSI/AAMI ST67. This part of ISO 11137 does not specify a quality management system for the control of all stages of production of medical devices.
VDI 2168 - LIFTS - PERSONNEL QUALIFICATION Organization: VDI
Date: 2007-04-01
Description: The following documents were taken into consideration: Lifts Directive 95/16/EC and Machinery Directive 98/37/EC Equipment and Product Safety Act as well as the 9th and 12th ordinances to the same Health and Safety at Work Act Operational Safety Ordinance – BetrSichV Maintenance instructions for lift systems as per EN 13015 Information issued by the employers' liability insurance associations Requirements set by the quality management systems (ISO 9001) The guideline describes contents and basic conditions of trainings suitable for qualification for: planning commissioning periodic testing product testing testing of services testing of lifts in their function as work equipment and as workplace The training offered addresses personnel of the NB1) personnel of the approved inspection institution2) qualified persons as specified in the technical rules complementing the BetrSichV and in TRBS 1203 et seq.
NR/L1/ADG/001 ISSUE 1 - ASSET DATA POLICY - COMPLIANCE DATE: 4 MARCH 2017 Organization: NR
Date: 2016-12-03
Description: c) processes: embedding processes across the asset management enterprise: 1) data operations; 2) data quality monitoring; and 3) data quality improvement. d) risk management: as part of the operations of a safety-critical organisation, using data to understand the risks based upon asset information so that corrective and mitigating actions can be taken.
ASTM E1579 - STANDARD GUIDE FOR ENSURING DATA INTEGRITY IN HIGHLY COMPUTERIZED LABORATORY OPERATIONS Organization: ASTM
Date: 1994-10-15
Description: 1.4 In highly computerized laboratories, computers are increasingly being used for: 1.4.1 Direct capture of data from instruments and testing machines; 1.4.2 Automatic control and monitoring of test processes; 1.4.3 Control of critical environmental conditions; 1.4.4 Capture, processing, and display of laboratory quality-control data; 1.4.5 Basic data processing; 1.4.6 Data storage and retrieval; 1.4.7 Generation of test reports; 1.4.8 Scheduling and monitoring of work throughput; 1.4.9 Monitoring and control of inventories; 1.4.10 Equipment inventories, and calibration and maintenance schedules; 1.4.11 Design of statistical experiments; and 1.4.12 Communication between laboratories (and with clients).
NPFC - DI-SESS-81924 - PROCESS REVIEW REPORT Organization: NPFC
Date: 2013-07-10
Description: Some examples of third-party quality standards to which this DID could apply are as follows: ISO9001 (Quality Management Systems – Requirements), ISO/IEC17025 (General Requirements for the Competence of Testing and Calibration Laboratories), ANSI/ISO/ASQ Q9001 (Quality Management Systems − Requirements), and SAE AS9100 (Quality Management Systems: Aerospace Requirements).
ASTM D6061 - STANDARD PRACTICE FOR EVALUATING THE PERFORMANCE OF RESPIRABLE AEROSOL SAMPLERS Organization: ASTM
Date: 2001-10-10
Description: When a health effects assessment has been based on a specific convention it is appropriate to use that same convention for setting permissible exposure limits in the workplace and ambient environment and for monitoring compliance. The conventions, which define inhalable, thoracic, and respirable aerosol sampler ideals, have now been adopted by the International Standards Organization (ISO 7708), the Comité Européen de Normalisation (CEN Standard EN 481), and the American Conference of Governmental Industrial Hygienists (ACGIH, Ref (1)),2 developed (2) in part from healtheffects studies reviewed in Ref (3) and in part as a compromise between definitions proposed in Refs (3,4).

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