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ASME - ANSI N45.2.1 - CLEANING OF FLUID SYSTEMS AND ASSOCIATED COMPONENTS FOR NUCLEAR POWER PLANTS (SEE ALSO NQA-1 AND NQA-2) Organization: ASME
Date: 1980-01-01
Description: This Standard covers the management of cleaning and cleanness control of fluid systems and associated components for nuclear power plants during manufacturing, construction, repairs, and modifications.
ASME NQA-1 - QUALITY ASSURANCE REQUIREMENTS FOR NUCLEAR FACILITY APPLICATIONS - INCLUDES INTERPRETATIONS NOVEMBER 2012 THROUGH NOVEMBER 2013 Organization: ASME
Date: 2015-02-20
Description: The Standard focuses on the achievement of results, emphasizes the role of the individual and line management in the achievement and sustainment of quality, and fosters the application of these requirements in a manner consistent with the relative importance of the item or activity (i.e., a "graded approach").
ASSE/SAFE - ANSI ASSE Z9.9 - PORTABLE VENTILATION SYSTEMS Organization: ASSE/SAFE
Date: 2010-01-01
Description: This Standard covers components of portable ventilation systems, including: — air movers and their modes of power — other components of portable ventilation systems including entry hoods; duct, hose, and other conveying structures; air-cleaning equipment including filters and sorbent air-purifying devices; and air coolers and heaters.
SSPC QP 3 - CERTIFICATION STANDARD FOR SHOP APPLICATION OF COMPLEX PROTECTIVE COATING SYSTEMS Organization: SSPC
Date: 2010-09-23
Description: The requirements of this Standard are applied to the quality management system of a certified Firm independent of individual project requirement for Certification to this Standard.
AISC - 420 - CERTIFICATION STANDARD FOR SHOP APPLICATION OF COMPLEX PROTECTIVE COATING SYSTEMS Organization: AISC
Date: 2010-09-23
Description: The requirements of this Standard are applied to the quality management system of a certified Firm independent of individual project requirement for Certification to this Standard.
ISO DIS 25424 - STERILIZATION OF HEALTH CARE PRODUCTS - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: ISO
Date: 2017-01-12
Description: This standard does not specify a quality management system for the control of all stages of production of medical devices.
CEN - EN ISO 25424 - STERILIZATION OF MEDICAL DEVICES - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: CEN
Date: 2011-06-01
Description: This standard does not specify a quality management system for the control of all stages of production of medical devices.
SNV - SN EN ISO 25424 - STERILIZATION OF MEDICAL DEVICES - LOW TEMPERATURE STEAM AND FORMALDEHYDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: SNV
Date: 2011-09-01
Description: This standard does not specify a quality management system for the control of all stages of production of medical devices.
ISO 25424 - STERILIZATION OF MEDICAL DEVICES — LOW TEMPERATURE STEAM AND FORMALDEHYDE — REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES - FIRST EDITION Organization: ISO
Date: 2009-09-01
Description: This standard does not specify a quality management system for the control of all stages of production of medical devices.
SAE J2554 - (R) ENGINE INTAKE AIR WATER SEPARATION TEST PROCEDURE Organization: SAE
Date: 2017-02-01
Description: Once on the clean side of the filter, the contamination particles, precipitates, or consequential corrosion residue are able to enter the engine and cause damage to the engine and engine management systems. Third, water vapor or liquid in sufficient quantities can cause filter media degradation, even to the point of burst for condition of wet media at high pressure drops Experience has shown that engine intake air water separation systems, which perform on the order of 80% or higher efficiency, as measured by this procedure, will usually avoid water ingestion problems It is therefore desirable to provide a procedure for uniformly measuring the effectiveness of intake systems in separating or otherwise removing water from the intake system Actual field conditions will vary widely, and are difficult to duplicate.
ISO 11135 - STERILIZATION OF HEALTH-CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES - SECOND EDITION Organization: ISO
Date: 2014-07-15
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
DIN 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 (ISO 11135:2014) Organization: DIN
Date: 2014-10-01
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
CEN - 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 Organization: CEN
Date: 2014-07-01
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
SNV - SN 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 Organization: SNV
Date: 2014-10-01
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
AAMI 11135 - STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: AAMI
Date: 2014-01-01
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
NATO - AMEPP-4 - GUIDANCE FOR THE INTEGRATION OF MARTIME ENVIRONMENTAL PROTECTION (MEP) FUNCTIONAL REQUIREMENTS INTO A SHIP DESIGN - ED 2; INCORPORATES CHANGE 1: MAY 2003 Organization: NATO
Date: 1999-01-01
Description: CONTENT AND OBJECTIVES The purpose of this document is to provide general guidance to naval architects and marine system designers for integrating environmental compliance requirements into new ship designs with minimal adverse impacts on operational capabilities, readiness, safety, survivability and crew's quality of life. This document contains only the management policies, shipboard treatment possibilities, and some recommendations for different technologies.
AAMI ST58 - CHEMICAL STERILIZATION AND HIGH-LEVEL DISINFECTION IN HEALTH CARE FACILITIES Organization: AAMI
Date: 2013-01-01
Description: Inclusions This recommended practice specifically addresses a) work area design considerations for processing areas in which liquid chemical sterilization/high-level disinfection and gaseous chemical sterilization systems are used; b) staff qualifications, education, and other personnel considerations; c) criteria for selecting liquid chemical sterilization/high-level disinfection and gaseous chemical sterilization systems; d) decontamination and preparation of instruments; e) safety and efficacy considerations in the use of liquid chemical sterilization/high-level disinfection and gaseous chemical sterilization systems; f) storage and transport of sterilized or disinfected devices; g) quality control methods; and h) quality process improvement.
ASTM MNL20 - CORROSION TESTS AND STANDARDS: APPLICATION AND INTERPRETATION - 2ND EDITION Organization: ASTM
Date: 2005-01-01
Description: This section is greatly expanded and includes a unified numbering system for metals and alloys and their common names, standards terminology, a glossary of terms and acronyms, abbreviations and units symbols, International System of Units and matrix guide, general conversion tables, corrosion rate calculations and all necessary conversion factors, chemical and physical properties of materials, properties of water and moist air, chemical and electrolytic cleaning procedures for corrosion products, physical properties of gases, liquids and elements, and densities of metals and alloys.

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