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CRC - KE11274 - HANDBOOK FOR CRITICAL CLEANING : CLEANING AGENTS AND SYSTEMS, SECOND EDITION Organization: CRC
Date: 2011-04-04
Description: The first volume, Handbook for Critical Cleaning: Cleaning Agents and Systems, gives manufacturers a practical understanding of the variety and functions of cleaning chemistries and cleaning, rinsing, and drying equipment.
CRC - KE11275 - HANDBOOK FOR CRITICAL CLEANING : APPLICATIONS, PROCESSES, AND CONTROLS, SECOND EDITION Organization: CRC
Date: 2011-04-04
Description: If so, when and how? Cleaning is essential for proper performance, optimal quality, and increased sales.
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.
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.
CRC - KE20041 - NATURAL AND ENGINEERED SOLUTIONS FOR DRINKING WATER SUPPLIES : LESSONS FROM THE NORTHEASTERN UNITED STATES AND DIRECTIONS FOR GLOBAL WATERSHED MANAGEMENT Organization: CRC
Date: 2013-03-26
Description: Illuminating opportunities to develop a more integrated approach to municipal water system design, Natural and Engineered Solutions for Drinking Water Supplies: Lessons from the Northeastern United States and Directions for Global Watershed Management explores critical factors in the decision-making processes for municipal water system delivery. The book offers vital insights to help inform management decisions on drinking water supply issues in other global regions in our increasingly energy- and carbon-constrained world.
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.
CRC - E3035 - UNINTERRUPTIBLE POWER SUPPLIES AND ACTIVE FILTERS Organization: CRC
Date: 2004-10-28
Description: Power demands of medical facilities, data storage and information systems, emergency equipment, etc. require uninterrupted, high quality power. Uninterruptible power supplies (UPS) and active filters provide this delivery.
CRC - TRENDS IN FISH PROCESSING - TRENDS IN FISH PROCESSING TECHNOLOGIES Organization: CRC
Date: 2017-10-26
Description: It provides references to food safety management systems and food safety & quality indicators for processed fish in order to achieve an adequate level of protection.
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.
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.
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.
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; TO OBTAIN PLEASE CONTACT YOUR NATIONAL DEFENSE STANDARDIZATION OFFICE OR THE NATO STANDARDIZATION OFFICE WEBSITE: HTTP://NSO.NATO.INT/NSO, PHONE: +32 (0)2 – 707 5556, EMAIL: NSO@NSO.NATO.INT. FOR ADDITIONAL INFORMATION PLEASE SEE THE IHS MARKIT LETTER CONCERNING ACCESSING RESTRICTED NATO PUBLICATIONS 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.
CRC - LE1364 - SAMPLING AND SURVEYING RADIOLOGICAL ENVIRONMENTS Organization: CRC
Date: 2000-09-19
Description: Sampling and Surveying Radiological Environments addresses all of the major topics that will assist you in designing and implementing statistically defensible sampling programs in radiological environments, including: Summary of the major environmental laws and regulations that apply to radiological sites, and advice on regulatory interfacing · Internet addresses where you can find regulations pertaining to each States Theory of radiation detection and definitions of common radiological terminology Statistics and statistical software that apply to the environmental industry Details on commercially available radiological instrumentation and detection systems Building decontamination and decommissioning, radiological and chemical equipment decontamination procedures, and tank/drum/remote characterization Standard operating procedures for collecting environmental media samples Guidance on sample preparation, documentation, and shipment Guidance on data verification/validation, radiological data management, data quality assessment (DQA) · An electronic template to assist you in implementing the EPA's seven step DQO procedure and in the writing of a DQO Summary Report, and Sampling and Analysis Plan · Recommendations for developing a Sampling and Analysis Plan · Guidance on developing statistical sampling and survey designs Guidance on developing integrated sampling and survey designs Capabilities of various statistical sampling design software packages along with Internet addresses for web pages where statistical software can be downloaded at no cost to you Effectiveness of various scanning and direct measurement methods Sampling and Surveying Radiological Environments provides you with the most cost effective methods and technologies for sampling, characterizing, and remediating radiologically contaminated environments.

1 - 20 of 24 results