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ASTM STP538 - CLEANING STAINLESS STEEL Organization: ASTM
Date: 1973-01-01
Description: Cleanliness requirements in the chemical industry, and in the food industry— where cleaning-in-place procedures are employed—are also emphasized.
ASTM D5030 - STANDARD TEST METHOD FOR DENSITY OF SOIL AND ROCK IN PLACE BY THE WATER REPLACEMENT METHOD IN A TEST PIT - REINSTATED 2004 Organization: ASTM
Date: 2004-03-01
Description: A very careful assessment must be made as to whether or not the volume determined is representative of the in-place condition when this test method is used for clean, relatively uniform-sized particles 3 in. (75 mm) and larger.
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.
SAE J792 - SAE MANUAL ON BLAST CLEANING, INFORMATION REPORT Organization: SAE
Date: 1968-06-01
Description: As parts become more complex in size and shape,specialized cleaning becomes more and more necessary. Work in the development of abrasives, blasting equipment, processes,and standization goes on.
PIP PH414SD0E01 - HYGIENIC PROCESS MATERIAL SPECIFICATION 414SD0E01 316/316L STAINLESS STEEL, 0.000" C.A. HYGIENIC PRODUCT & CLEAN IN PLACE SYSTEMS SF4 ID FINISH, SF0 OD FINISH, FKM SEALS HYGIENIC CONSTRUCTION CLAMPED/JOINED UNIONS Organization: PIP
Date: 2015-04-01
Description: Determinations concerning fitness for purpose and particular matters or application of the Practice to particular project or engineering situations should not be made solely on information contained in these materials. The use of trade names from time to time should not be viewed as an expression of preference but rather recognized as normal usage in the trade.
PIP PH414SD0E02 - PIPING MATERIAL SPECIFICATION 414SD0E02 316/316L STAINLESS STEEL, 0.000" C.A. HYGIENIC PRODUCT & CLEAN IN PLACE SYSTEMS SF4 ID FINISH, SF0 OD FINISH, EPDM SEALS HYGIENIC CONSTRUCTION CLAMPED/JOINED UNIONS Organization: PIP
Date: 2015-04-01
Description: Determinations concerning fitness for purpose and particular matters or application of the Practice to particular project or engineering situations should not be made solely on information contained in these materials. The use of trade names from time to time should not be viewed as an expression of preference but rather recognized as normal usage in the trade.
ASME STP/PT-065 - BRANCH LEG STUDY FOR BIOPROCESSING EQUIPMENT Organization: ASME
Date: 2013-12-19
Description: When air is displaced from the branched fitting, the cleaning solution comes in contact with the branched piping components being cleaned-in-place (CIP'ed) and effective cleaning can occur.
IEST-RP-CC027 - PERSONNEL PRACTICES AND PROCEDURES IN CLEANROOMS AND CONTROLLED ENVIRONMENTS Organization: IEST
Date: 2006-04-01
Description: Also, because activities within the cleanroom can carry in, generate, stir up, or transfer contamination from place to place within the cleanroom, a system of operational protocols should be developed, enforced, and monitored to maintain the proper controls.
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.
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.
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.
ASTM F2542 - STANDARD TEST METHODS FOR PHYSICAL ASSAULT ON VENTILATION GRILLES FOR DETENTION AND CORRECTIONAL FACILITIES Organization: ASTM
Date: 2005-12-01
Description: When filter grilles are provided, filters shall have a minimum UL-900 class 2 rating, and a filter replacement program needs to be in place at the facility. Airflow performance shall be catalogued in accordance with ASHRAE 70–91.
PACKT - PYTHON BUSINESS INTELLIGE - PYTHON BUSINESS INTELLIGENCE COOKBOOK Organization: PACKT
Date: 2015-12-22
Description: If you have a good knowledge and understanding of BI applications and have a “working” system in place, this book will enhance your toolbox. What You Will Learn • Install Anaconda, MongoDB, and everything you need to get started with your data analysis • Prepare data for analysis by querying cleaning and standardizing data • Explore your data by creating a Pandas data frame from MongoDB • Gain powerful insights, both statistical and predictive, to make informed business decisions • Visualize your data by building dashboards and generating reports • Create a complete data processing and business intelligence system In Detail The amount of data produced by businesses and devices is going nowhere but up.
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.
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.
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.
SSPC TU 7 - CONDUCTING AMBIENT AIR, SOIL, AND WATER SAMPLING OF SURFACE PREPARATION AND PAINT DISTURBANCE ACTIVITIES Organization: SSPC
Date: 2015-05-04
Description: STATEMENT OF PURPOSE This technology update describes methods and equipment used for assessing emissions during surface preparation and other emission generating operations and to assess whether the controls in place are adequate for protecting the public, the environment, and adjacent personnel or meeting federal, state and local regulations or specified requirements.
ITU-R REPORT RS.2178 - THE ESSENTIAL ROLE AND GLOBAL IMPORTANCE OF RADIO SPECTRUM USE FOR EARTH OBSERVATIONS AND FOR RELATED APPLICATIONS Organization: ITU-R
Date: 2010-10-01
Description: National Research Council, concluded in 2007 in its publication "Earth science and applications from space: National imperatives for the next decade and beyond," as follows: "The world faces significant environmental challenges: shortages of clean and accessible freshwater, degradation of terrestrial and aquatic ecosystems, increases in soil erosion, changes in chemistry of the atmosphere, declines in fisheries, and the likelihood of substantial changes in climate.

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