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SAE J792 - SAE MANUAL ON BLAST CLEANING, INFORMATION REPORT Organization: SAE
Date: 1968-06-01
Description: However,the high operational cost and low productivity of the process at thattime limited its use to the cleaning of large castings or productswhere high quality was necessary regardless of cost.
API/EI 1585 - GUIDANCE IN THE CLEANING OF AVIATION FUEL HYDRANT SYSTEMS AT AIRPORTS - SECOND EDITION; NOW COPYRIGHTED BY EI Organization: API
Date: 2007-11-01
Description: It cannot be too strongly stressed that the key is to ensure that the hydrant system is clean in the first place.
PACKT - MASTERING SOFTWARE TESTIN - MASTERING SOFTWARE TESTING WITH JUNIT 5 Organization: PACKT
Date: 2017-10-27
Description: What You Will Learn • The importance of software testing and its impact on software quality • The options available for testing Java applications • The architecture, features and extension model of JUnit 5 • Writing test cases using the Jupiter programming model • How to use the latest and advanced features of JUnit 5 • Integrating JUnit 5 with existing third-party frameworks • Best practices for writing meaningful JUnit 5 test cases • Managing software testing activities in a living software project In Detail When building an application it is of utmost importance to have clean code, a productive environment and efficient systems in place. Having automated unit testing in place helps developers to achieve these goals.
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: NOTE It is not a requirement of this standard to have a complete quality management system during manufacture or reprocessing, but those elements of such a system that are required are normatively referenced at appropriate places in the text. Attention is drawn to the standards for quality management systems (see ISO 13485) that control all stages of production or reprocessing of medical devices including the sterilization process.
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: NOTE It is not a requirement of this standard to have a complete quality management system during manufacture or reprocessing, but those elements of such a system that are required are normatively referenced at appropriate places in the text. Attention is drawn to the standards for quality management systems (see EN ISO 13485) that control all stages of production or reprocessing of medical devices including the sterilization process.
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: NOTE It is not a requirement of this standard to have a complete quality management system during manufacture or reprocessing, but those elements of such a system that are required are normatively referenced at appropriate places in the text. Attention is drawn to the standards for quality management systems (see EN ISO 13485) that control all stages of production or reprocessing of medical devices including the sterilization process.
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: NOTE It is not a requirement of this standard to have a complete quality management system during manufacture or reprocessing, but those elements of such a system that are required are normatively referenced at appropriate places in the text. Attention is drawn to the standards for quality management systems (see EN ISO 13485) that control all stages of production or reprocessing of medical devices including the sterilization process.
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: The necessary elements are normatively referenced at appropriate places in the text (see, in particular, Clause 4). Attention is drawn to the standards for quality management systems (see ISO 13485) that control all stages of production or reprocessing of medical devices.
DIN - 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: The necessary elements are normatively referenced at appropriate places in the text (see, in particular, Clause 4). Attention is drawn to the standards for quality management systems (see ISO 13485) that control all stages of production or reprocessing of medical devices.
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: The necessary elements are normatively referenced at appropriate places in the text (see, in particular, Clause 4). Attention is drawn to the standards for quality management systems (see ISO 13485) that control all stages of production or reprocessing of medical devices.
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: The necessary elements are normatively referenced at appropriate places in the text (see, in particular, Clause 4). Attention is drawn to the standards for quality management systems (see ISO 13485) that control all stages of production or reprocessing of medical devices.
SSPC TU 7 - CONDUCTING AMBIENT AIR, SOIL, AND WATER SAMPLING OF SURFACE PREPARATION AND PAINT DISTURBANCE ACTIVITIES Organization: SSPC
Date: 2015-05-04
Description: REGULATIONS: The primary federal regulations currently addressing exposures to hazardous and toxic substances, fugitive emissions of dust include: the Clean Air Act (CAA), and all amendments such as the National Ambient Air Quality Standards (NAAQS) for airborne lead, particulate matter with an aerodynamic diameter of less than ten (10) and two and one-half (2.5) micrometers (PM-10 and PM-2.5), the Resource Conservation and Recovery Act (RCRA) and the Comprehensive Environmental Response, Compensation and Liability Act (CERCLA), all mandated by the Environmental Protection Agency (EPA), and the current Occupational Safety and Health Administration (OSHA) General Industry, Shipyard, and Construction Industry Comprehensive Health Standards for Lead, Cadmium, Arsenic, Hexavalent Chromium, and other constituents that are present in or on substrates, coatings, and abrasives.
ASHRAE 90432 - ADVANCED ENERGY DESIGN GUIDE FOR SMALL RETAIL BUILDINGS: 30% ENERGY SAVINGS Organization: ASHRAE
Date: 2006-01-01
Description: Plans are in place for development of additional AEDG documents in this decade that will assist users in achieving 50% and 70% energy-saving levels as milestones toward the NZEB goal.
API PUBL 304 - EVALUATION OF RESTORATION ALTERNATIVES FOR NATURAL RESOURCES INJURED BY OIL SPILLS Organization: API
Date: 1991-08-01
Description: For example: · Injury means a measurable adverse change, either long- or short-term, in the chemical or physical quality or the viability of a natural resource, resulting either directly or indirectly from exposure to a discharge of oil [43 CFR § 11.14(v)].

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