DIN EN ISO 29701:2011-01
|
Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010) |
IEC/IEEE 62659:2015
|
Nanomanufacturing - Large scale manufacturing for nanoelectronics |
PD CEN ISO/TS 80004-6:2015
|
Nanotechnologies. Vocabulary Nano-object characterization |
06/30155554 DC : DRAFT AUG 2006
|
ISO 18938 - IMAGING MATERIALS - OPTICAL DISCS - CARE AND HANDLING FOR EXTENDED STORAGE |
05/30137700 DC : DRAFT AUG 2005
|
ISO 21501-4 - DETERMINATION OF PARTICLE SIZE DISTRIBUTION - SINGLE PARTICLE LIGHT-INTERACTION METHODS - PART 4: LIGHT-SCATTERING AIRBORNE PARTICLE COUNTER FOR CLEAN SPACES |
13/30283691 DC : 0
|
BS EN ISO 1135-4 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED |
13/30281604 DC : 0
|
BS ISO 14706 - SURFACE CHEMICAL ANALYSIS - DETERMINATION OF SURFACE ELEMENTAL CONTAMINATION ON SILICON WAFERS BY TOTAL-REFLECTION X-RAY FLUORESCENCE (TXRF) SPECTROSCOPY |
BS ISO 19924:2017
|
Space systems. Acoustic testing |
04/30098089 DC : DRAFT APR 2004
|
ISO 16232-4 - ROAD VEHICLES - CLEANLINESS OF COMPONENTS OF FLUID CIRCUITS - PART 4: METHOD OF EXTRACTION OF CONTAMINANTS BY ULTRASONIC TECHNIQUES |
08/30184486 DC : DRAFT JUNE 2008
|
BS EN ISO 1135-4 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE |
BS EN 16602-70-55:2015
|
Space product assurance. Microbiological examination of flight hardware and cleanrooms |
BS EN 16603-20-08:2014
|
Space engineering Photovoltaic assemblies and components |
I.S. EN 13824:2005
|
STERILIZATION OF MEDICAL DEVICES - ASEPTIC PROCESSING OF LIQUID MEDICAL DEVICES - REQUIREMENTS |
AAMI TIR52 : 2014(R2017)
|
ENVIRONMENTAL MONITORING FOR TERMINALLY STERILIZED HEALTHCARE PRODUCTS |
CEN ISO/TS 80004-6:2015
|
NANOTECHNOLOGIES - VOCABULARY - PART 6: NANO-OBJECT CHARACTERIZATION (ISO/TS 80004-6:2013) |
BS PD ISO/TS 80004-6 : 2013
|
NANOTECHNOLOGIES - VOCABULARY - PART 6: NANO-OBJECT CHARACTERIZATION |
I.S. CLC/TR 62258-3:2007
|
SEMICONDUCTOR DIE PRODUCTS - PART 3: RECOMMENDATIONS FOR GOOD PRACTICE IN HANDLING, PACKING AND STORAGE |
02/564514 DC : DRAFT OCT 2002
|
BS EN ISO 8536-4 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
BS EN 16602-70-08:2015
|
Space product assurance. Manual soldering of high-reliability electrical connections |
04/30110525 DC : DRAFT MARCH 2004
|
IEC 62258-3 ED.1 - SEMICONDUCTOR DIE PRODUCTS - PART 3 - RECOMMENDATIONS FOR GOOD PRACTICE IN HANDLING, PACKING AND STORAGE |
14/30287226 DC : 0
|
BS EN ISO 15378 - PRIMARY PACKAGING MATERIALS FOR MEDICINAL PRODUCTS - PARTICULAR REQUIREMENTS FOR THE APPLICATION OF ISO 9001:2008, WITH REFERENCE TO GOOD MANUFACTURING PRACTICE (GMP) |
BS EN ISO 24998:2008
|
Plastics laboratory ware. Single-use Petri dishes for microbiological procedures |
BS ISO 18938:2014
|
Imaging materials. Optical discs. Care and handling for extended storage |
07/19969755 DC : 0
|
BS ISO 11500 - HYDRAULIC FLUID POWER - DETERMINATION OF PARTICULATE CONTAMINATION LEVEL OF A LIQUID SAMPLE BY AUTOMATIC PARTICLE COUNTING USING THE LIGHT EXTINCTION PRINCIPLE |
04/30098086 DC : DRAFT APR 2004
|
ISO 16232-3 - ROAD VEHICLES - CLEANLINESS OF COMPONENTS OF FLUID CIRCUITS - PART 3: METHOD OF EXTRACTION OF CONTAMINANTS BY PRESSURE RINSING |
BS EN 62258-1:2010
|
Semiconductor die products Procurement and use |
BS EN ISO 14644-13:2017
|
Cleanrooms and associated controlled environments Cleaning of surfaces to achieve defined levels of cleanliness in terms of particle and chemical classifications |
I.S. EN ISO 14644-10:2013
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 10: CLASSIFICATION OF SURFACE CLEANLINESS BY CHEMICAL CONCENTRATION (ISO 14644-10:2013) |
BS ISO 13142:2015
|
Electro-optical systems. Cavity ring-down technique for high-reflectance measurement |
SEMI E146 : 2006
|
TEST METHOD FOR THE DETERMINATION OF PARTICULATE CONTAMINATION FROM MINIENVIRONMENTS USED FOR STORAGE AND TRANSPORT OF SILICON WAFERS |
BS ISO 16232-7:2007
|
Road vehicles. Cleanliness of components of fluid circuits Particle sizing and counting by microscopic analysis |
MIL-STD-750-3 Base Document:2012
|
Transistor Electrical Test Methods for Semiconductor Devices Part 3: Test Methods 3000 Through 3999 |
ASTM E 2311 : 2004 : R2016
|
Standard Practice for QCM Measurement of Spacecraft Molecular Contamination in Space |
CSA Z10083 : 2008
|
OXYGEN CONCENTRATOR SUPPLY SYSTEMS FOR USE WITH MEDICAL GAS PIPELINE SYSTEMS |
I.S. EN 16844:2017+A2:2019
|
Aesthetic medicine services - Non-surgical medical treatments |
AAMI ISO 13408-1 : 2008 : R2011
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 1: GENERAL REQUIREMENTS |
CAN/CSA-Z5100-17
|
Cellulose nanomaterials - Test methods for characterization |
ISO 16232-1:2007
|
Road vehicles Cleanliness of components of fluid circuits Part 1: Vocabulary |
I.S. EN ISO 1135-5:2015
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 1135-5:2015) |
ISO 8871-3:2003
|
Elastomeric parts for parenterals and for devices for pharmaceutical use Part 3: Determination of released-particle count |
AAMI/ISO TIR17665-3:2014(R2016)
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - GUIDANCE ON THE DESIGNATION OF A MEDICAL PRODUCT TO A PRODUCT FAMILY AND PROCESSING CATEGORY FOR STEAM STERILIZATION |
I.S. EN 16602-70-58:2015
|
SPACE PRODUCT ASSURANCE - BIOBURDEN CONTROL OF CLEANROOMS |
ISO 15378:2017
|
Primary packaging materials for medicinal products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) |
I.S. EN 62258-1:2010
|
SEMICONDUCTOR DIE PRODUCTS - PART 1: PROCUREMENT AND USE |
ISO 20188:2018
|
Space systems — Product assurance requirements for commercial satellites |
BS EN ISO 7396-1:2016
|
Medical gas pipeline systems Pipeline systems for compressed medical gases and vacuum |
GOST ISO 14698-1 : 2005
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL - PART 1: GENERAL PRINCIPLES AND METHODS |
NASA MSFC SPEC 1238 : 2007
|
THERMAL VACUUM BAKEOUT SPECIFICATION FOR CONTAMINATION SENSITIVE HARDWARE |
I.S. EN ISO 14644-15:2017
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 15: ASSESSMENT OF SUITABILITY FOR USE OF EQUIPMENT AND MATERIALS BY AIRBORNE CHEMICAL CONCENTRATION (ISO 14644-15:2017) |
UNI EN ISO 13408-6 : 2013
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 6: ISOLATOR SYSTEMS |
ISO 18913:2012
|
Imaging materials Permanence Vocabulary |
DIN EN ISO 14644-13:2016-03 (Draft)
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 13: CLEANING OF SURFACES TO ACHIEVE DEFINED LEVELS OF CLEANLINESS IN TERMS OF PARTICLE AND CHEMICAL CLASSIFICATIONS (ISO 14644-13:2017) |
UNE-EN ISO 1135-3:2017
|
Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016) |
ASTM E 1549/E1549M : 2013
|
Standard Specification for ESD Controlled Garments Required in Cleanrooms and Controlled Environments for Spacecraft for Non-Hazardous and Hazardous Operations |
ISO 10083:2006
|
Oxygen concentrator supply systems for use with medical gas pipeline systems |
ASTM E 2088 : 2006
|
Standard Practice for Selecting, Preparing, Exposing, and Analyzing Witness Surfaces for Measuring Particle Deposition in Cleanrooms and Associated Controlled Environments |
ASTM E 2217 : 2012 : REDLINE
|
Standard Practice for Design and Construction of Aerospace Cleanrooms and Contamination Controlled Areas |
ASTM F 2332 : 2006
|
Standard Specification for Annular Ball Bearings for Instruments and Precision Rotating Components |
ASTM F 2444 : 2004
|
Standard Practice for Damage Prevention of Bearings, and Bearing Components Through Proper Handling Techniques |
ASTM E 2088 : 2006 : R2011
|
Standard Practice for Selecting, Preparing, Exposing, and Analyzing Witness Surfaces for Measuring Particle Deposition in Cleanrooms and Associated Controlled Environments |
ISO 19724:2016
|
Gasoline engines with direct injection Cleanliness assessment of fuel injection equipment |
ASTM G 93 : 2003 : R2011
|
Standard Practice for Cleaning Methods and Cleanliness Levels for Material and Equipment Used in Oxygen-Enriched Environments |
NFPA 318 : 2018
|
PROTECTION OF SEMICONDUCTOR FABRICATION FACILITIES |
I.S. EN ISO 14644-3:2006
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 3: TEST METHODS |
EN ISO 8536-4:2013/A1:2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010/AMD 1:2013) |
DIN EN ISO 14698-1 E : 2004
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL - PART 1: GENERAL PRINCIPLES AND METHODS |
MIL-STD-883 Revision K:2016
|
TEST METHOD STANDARD - MICROCIRCUITS |
BS ISO 16232-10:2007
|
Road vehicles. Cleanliness of components of fluid circuits Expression of results |
BS EN ISO 13697:2006
|
Optics and photonics. Lasers and laser-related equipment. Test methods for specular reflectance and regular transmittance of optical laser components |
BS EN ISO 14644-2:2015
|
Cleanrooms and associated controlled environments Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration |
BS EN ISO 14644-6:2007
|
Cleanrooms and associated controlled environments Vocabulary |
ISO 14644-7:2004
|
Cleanrooms and associated controlled environments — Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments) |
BS EN ISO 9073-10:2004
|
Textiles. Test methods for nonwovens Lint and other particles generation in the dry state |
ISO 13408-1:2008
|
Aseptic processing of health care products — Part 1: General requirements |
BS EN 13824:2004
|
Sterilization of medical devices. Aseptic processing of liquid medical devices. Requirements |
CLC/TR 62258-3:2007
|
Semiconductor die products - Part 3: Recommendations for good practice in handling, packing and storage |
DIN EN ISO 13696:2002-12
|
Optics and optical instruments - Test methods for radiation scattered by optical components (ISO 13696:2002) |
CEN ISO/TR 14969:2005
|
Medical devices - Quality management systems - Guidance on the application of ISO 13485:2003 (ISO/TR 14969:2004) |
EN 62258-1:2010
|
Semiconductor die products - Part 1: Procurement and use |
DIN EN ISO 14698-1:2004-04
|
Cleanrooms and associated controlled environments - Biocontamination control - Part 1: General principles and methods (ISO 14698-1:2003) |
I.S. EN ISO 24013:2006
|
OPTICS AND PHOTONICS - LASERS AND LASER-RELATED EQUIPMENT - MEASUREMENT OF PHASE RETARDATION OF OPTICAL COMPONENTS FOR POLARIZED LASER RADIATION |
MIL STD 750-2 : A
|
MECHANICAL TEST METHODS FOR SEMICONDUCTOR DEVICES - PART 2: TEST METHODS 2001 THROUGH 2999 |
ONORM EN ISO 14644-10 : 2013
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 10: CLASSIFICATION OF SURFACE CLEANLINESS BY CHEMICAL CONCENTRATION (ISO 14644-10:2013) |
BS EN ISO 15378:2017
|
Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) |
NF EN ISO 5667-23 : 2011
|
WATER QUALITY - SAMPLING - PART 23: GUIDANCE ON PASSIVE SAMPLING IN SURFACE WATERS |
06/30160058 DC : 0
|
BS EN ISO 8536-4 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
10/30207686 DC : DRAFT DEC 2010
|
BS ISO 12345 - DIESEL ENGINES - CLEANLINESS ASSESSMENT OF FUEL INJECTION EQUIPMENT |
03/301960 DC : DRAFT MAR 2003
|
ISO 18933 - IMAGING MATERIALS - MAGNETIC TAPE - CARE AND HANDLING PRACTICES FOR EXTENDED USAGE |
BS EN 16442:2015
|
Controlled environment storage cabinet for processed thermolabile endoscopes |
EN ISO 8871-3:2004
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICALS USE - PART 3: DETERMINATION OF RELEASED-PARTICLE COUNT |
PD CLC/TR 62258-3:2007
|
Semiconductor die products Recommendations for good practice in handling, packing and storage |
16/30337963 DC : 0
|
BS ISO 20437 - NATURAL RUBBER LATEX CLEANROOM GLOVES - SPECIFICATION |
ASTM F 1708 : 2002
|
Standard Practice for Evaluation of Granular Polysilicon by Meter-Zoner Spectroscopies (Withdrawn 2003) |
PREN ISO 14644-2 : DRAFT 2010
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 2: SPECIFICATIONS FOR MONITORING AND PERIODIC TESTING TO PROVE CONTINUED COMPLIANCE WITH ISO 14644-1 |
ISO 4407:2002
|
Hydraulic fluid power — Fluid contamination — Determination of particulate contamination by the counting method using an optical microscope |
PD ISO/TR 18196:2016
|
Nanotechnologies. Measurement technique matrix for the characterization of nano-objects |
MIL-STD-790 Revision G:2011
|
ESTABLISHED RELIABILITY AND HIGH RELIABILITY QUALIFIED PRODUCTS LIST (QPL) SYSTEMS FOR ELECTRICAL, ELECTRONIC, AND FIBER OPTIC PARTS SPECIFICATIONS |
99/124125 DC : DRAFT NOV 1999
|
BS EN ISO 15883-1 - WASHER-DISINFECTORS - PART 1: GENERAL REQUIREMENTS, DEFINITIONS AND TESTS |
ISO 18933:2012
|
Imaging materials Magnetic tape Care and handling practices for extended usage |
DIN EN ISO 1135-5:2016-06
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 1135-5:2015) |
16/30295652 DC : 0
|
BS EN ISO 14644-15 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 15: ASSESSMENT OF SUITABILITY FOR USE OF EQUIPMENT AND MATERIALS BY AIRBORNE CHEMICAL AND SURFACE CHEMICAL CONCENTRATION |
BS EN 16602-70-58:2015
|
Space product assurance. Bioburden control of cleanrooms |
DIN EN ISO 13408-6:2013-07
|
Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005 + Amd 1:2013) (includes Amendment A1:2013) |
BS ISO 15378 : 2006 AMD 17315
|
PRIMARY PACKAGING MATERIALS FOR MEDICINAL PRODUCTS - PARTICULAR REQUIREMENTS FOR THE APPLICATION OF ISO 9001:2000, WITH REFERENCE TO GOOD MANUFACTURING PRACTICE (GMP) |
14/30271334 DC : 0
|
BS ISO 13142 - ELECTRO-OPTICAL SYSTEMS - CAVITY RING-DOWN TECHNIQUE FOR HIGH-REFLECTANCE MEASUREMENT |
PD ISO/TS 17665-3:2013
|
Sterilization of health care products. Moist heat Guidance on the designation of a medical device to a product family and processing category for steam sterilization |
02/123800 DC : DRAFT OCT 2002
|
BS EN ISO 14644-3 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 3: METROLOGY AND TEST METHODS |
EN ISO 7396-1:2016
|
Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2016) |
14/30303657 DC : 0
|
BS EN ISO 1135-3 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SET FOR SINGLE USE |
13/30278952 DC : 0
|
BS EN 16372 - AESTHETIC SURGERY AND AESTHETIC NON-SURGICAL MEDICAL SERVICES |
ASTM E 2311 : 2004
|
Standard Practice for QCM Measurement of Spacecraft Molecular Contamination in Space |
DIN EN ISO 13408-1:2015-12
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 1: GENERAL REQUIREMENTS (ISO 13408-1:2008, INCLUDING AMD 1:2013) |
DIN 50451-1:2003-04
|
Determination of trace elements in liquids for use in semiconductor technology - Part 1: Determination of calcium, copper, gold, iron, potassium, silver and sodium in nitric acid by atomic absorption spectrometry |
DIN ISO 11040-4 E : 2017
|
PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015) |
MIL-DTL-197 Revision M:2016
|
PACKAGING OF BEARINGS, ASSOCIATED PARTS AND SUBASSEMBLIES |
DIN EN ISO 1135-5 E : 2016
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 1135-5:2015) |
CSA Z17665-2:09 (R2019)
|
Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (Adopted ISO/TS 17665-2:2009, first edition, 2009-01-15) |
04/30066665 DC : DRAFT MARCH 2004
|
BS ISO 13408-6 - ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 6 - ISOLATOR SYSTEMS |
BS ISO 21501-4:2007
|
Determination of particle size distribution. Single particle light interaction methods Light scattering airborne particle counter for clean spaces |
BS ISO 18933:2012
|
Imaging materials. Magnetic tape. Care and handling practices for extended usage |
ASTM E 2090 : 2012 : REDLINE
|
Standard Test Method for Size-Differentiated Counting of Particles and Fibers Released from Cleanroom Wipers Using Optical and Scanning Electron Microscopy |
I.S. EN 16844:2017
|
AESTHETIC MEDICINE SERVICES - NON-SURGICAL MEDICAL PROCEDURES |
MIL-DTL-24784-7 Revision D:2017
|
Technical Repair Standards (TRS) for Hull, Mechanical, and Electrical (HM&E) Equipment, Electronic Equipment, and Ordnance Equipment |
BS ISO 16232-3:2007
|
Road vehicles. Cleanliness of components of fluid circuits Method of extraction of contaminants by pressure rinsing |
ISO 13142:2015
|
Electro-optical systems Cavity ring-down technique for high-reflectance measurement |
S.R. CEN ISO/TS 80004-6:2015
|
NANOTECHNOLOGIES - VOCABULARY - PART 6: NANO-OBJECT CHARACTERIZATION (ISO/TS 80004-6:2013) |
AAMI ST67 : 2011
|
STERILIZATION OF HEALTH CARE PRODUCTS - REQUIREMENTS AND GUIDANCE FOR SELECTING A STERILITY ASSURANCE LEVEL (SAL) FOR PRODUCTS LABELED 'STERILE' |
UNI CEN ISO/TS 17665-2 : 2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ISO 17665-1 |
UNE-EN ISO 15378:2016
|
Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP) (ISO 15378:2015) |
UNE-EN ISO 13408-6:2011
|
Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005) |
BS EN ISO 13408-1:2015
|
Aseptic processing of health care products General requirements |
I.S. EN ISO 8871-3:2004
|
ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICALS USE - PART 3: DETERMINATION OF RELEASED-PARTICLE COUNT |
AAMI ISO 11737-2 : 2009 : R2014
|
STERILIZATION OF MEDICAL DEVICES - MICROBIOLOGICAL METHODS - PART 2: TESTS OF STERILITY PERFORMED IN THE DEFINITION, VALIDATION AND MAINTENANCE OF A STERILIZATION PROCESS |
I.S. EN 16602-70-55:2015
|
SPACE PRODUCT ASSURANCE - MICROBIOLOGICAL EXAMINATION OF FLIGHT HARDWARE AND CLEANROOMS |
ISO 19924:2017
|
Space systems — Acoustic testing |
AAMI ISO 11737-2 :2009
|
STERILIZATION OF MEDICAL DEVICES - MICROBIOLOGICAL METHODS - PART 2: TESTS OF STERILITY PERFORMED IN THE DEFINITION, VALIDATION AND MAINTENANCE OF A STERILIZATION PROCESS |
BS EN ISO 13408-6 : 2011
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 6: ISOLATOR SYSTEMS |
UNE-EN ISO 1135-5:2016
|
Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015) |
I.S. EN ISO 14644-14:2016
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 14: ASSESSMENT OF SUITABILITY FOR USE OF EQUIPMENT BY AIRBORNE PARTICLE CONCENTRATION (ISO/DIS 14644-14) |
DIN EN ISO 14644-10:2013-06
|
Cleanrooms and associated controlled environments - Part 10: Classification of surface cleanliness by chemical concentration (ISO 14644-10:2013) |
GOST ISO 14698-2 : 2005
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL - PART 2: EVALUATION AND INTERPRETATION OF BIOCONTAMINATION DATA |
CSA Z17665-2:09 (R2019)
|
Sterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1 (ISO/TS 17665-2:2009, IDT) |
BS EN ISO 14644-15:2017
|
Cleanrooms and associated controlled environments Assessment of suitability for use of equipment and materials by airborne chemical concentration |
I.S. EN ISO 5667-23:2011
|
WATER QUALITY - SAMPLING - PART 23: GUIDANCE ON PASSIVE SAMPLING IN SURFACE WATERS |
I.S. EN ISO 13408-6:2011
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 6: ISOLATOR SYSTEMS (ISO 13408-6:2005) |
EN ISO 14644-13:2017
|
Cleanrooms and associated controlled environments - Part 13: Cleaning of surfaces to achieve defined levels of cleanliness in terms of particle and chemical classifications (ISO 14644-13:2017) |
ASTM E 2352 : 2019
|
Standard Practice for Aerospace Cleanrooms and Associated Controlled Environments—Cleanroom Operations |
ASTM E 2042 : 2004
|
Standard Practice for Cleaning and Maintaining Controlled Areas and Clean Rooms |
ASTM E 1548 : 2009 : R2017
|
Standard Practice for Preparation of Aerospace Contamination Control Plans |
ASTM E 2352 : 2004
|
Standard Practice for Aerospace Cleanrooms and Associated Controlled Environments-Cleanroom Operations |
UNI EN ISO 29701 : 2010
|
NANOTECHNOLOGIES - ENDOTOXIN TEST ON NANOMATERIAL SAMPLES FOR IN VITRO SYSTEMS - LIMULUS AMEBOCYTE LYSATE (LAL) TEST |
I.S. EN 16442:2015
|
CONTROLLED ENVIRONMENT STORAGE CABINET FOR PROCESSED THERMOLABILE ENDOSCOPES |
ASTM E 3059 : 2016
|
Standard Guide for Workforce Education in Nanotechnology Infrastructure |
ASTM E 1548 : 2009
|
Standard Practice for Preparation of Aerospace Contamination Control Plans |
ASTM E 2042/E2042M : 2009
|
Standard Practice for Cleaning and Maintaining Controlled Areas and Clean Rooms |
ASTM F 50 : 2012 : R2015
|
Standard Practice for Continuous Sizing and Counting of Airborne Particles in Dust-Controlled Areas and Clean Rooms Using Instruments Capable of Detecting Single Sub-Micrometre and Larger Particles |
DIN EN ISO 1135-4:2016-06
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015) |
DIN EN ISO 24013:2007-02
|
Optics and photonics - Lasers and laser-related equipment - Measurement of phase retardation of optical components for polarized laser radiation (ISO 24013:2006) |
ISO 14644-6:2007
|
Cleanrooms and associated controlled environments Part 6: Vocabulary |
BS EN ISO 11737-2:2009
|
Sterilization of medical devices. Microbiological methods Tests of sterility performed in the definition, validation and maintenance of a sterilization process |
ISO 13408-6:2005
|
Aseptic processing of health care products Part 6: Isolator systems |
BS EN ISO 14644-4:2001
|
Cleanrooms and associated controlled environments Design, construction and start-up |
UNE-EN ISO 8536-4:2013
|
Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed (ISO 8536-4:2010) |
BS EN ISO 14698-1:2003
|
Cleanrooms and associated controlled environments. Biocontamination control General principles and methods |
I.S. EN ISO 1135-4:2015
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015) |
I.S. EN 131-2:2010
|
LADDERS - PART 2: REQUIREMENTS, TESTING, MARKING |
I.S. EN ISO 14644-6:2007
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 6: VOCABULARY |
DIN EN ISO 11551:2004-05
|
OPTICS AND OPTICAL INSTRUMENTS - LASERS AND LASER-RELATED EQUIPMENT - TEST METHOD FOR ABSORPTANCE OF OPTICAL LASER COMPONENTS |
UNI EN ISO 11737-2 : 2010
|
STERILIZATION OF MEDICAL DEVICES - MICROBIOLOGICAL METHODS - PART 2: TESTS OF STERILITY PERFORMED IN THE DEFINITION, VALIDATION AND MAINTENANCE OF A STERILIZATION PROCESS |
I.S. EN ISO 14698-1:2003
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL - PART 1: GENERAL PRINCIPLES AND METHODS |
VDI 2083 Blatt 17:2013-06
|
Cleanroom technology - Compatibility of materials with the required cleanliness |
VDI 2083 Blatt 15:2007-04
|
Cleanroom technology - Personnel at the clean work place |
VDI 4066 Blatt 1:2013-05
|
Hygienic requirements for the production and aseptically filling of beverage products - Principles and design criteria |
VDI 2083 Blatt 8.1:2014-10
|
Cleanroom technology - Air cleanliness chemical concentration (ACC) |
VDI 2083 Blatt 9.2:2017-01
|
Cleanroom technology - Consumables in the cleanroom |
VDI 2083 Blatt 16.2:2015-10 (Draft)
|
Cleanroom technology - Barrier systems - Mini-environments |
VDI 2083 Blatt 1:2013-01
|
Cleanroom technology - Particulate air cleanliness classes |
MIL-DTL-197 Revision N:2022
|
Packaging of Bearings, Associated Parts and Subassemblies |
VDI 2083 Blatt 3:2005-07
|
Cleanroom technology - Metrology and test methods |
VDI/VDE 2627 Blatt 1:2015-12
|
Measuring rooms - Classification and characteristics - Planning and execution |
VDI 2083 Blatt 13.2:2009-01
|
Cleanroom technology - Quality, production and distribution of ultrapure water - Microelectronics and other technical applications |
VDI 2083 Blatt 13.1:2009-01
|
Cleanroom technology - Quality, production and distribution of ultrapure water - Fundamentals |
VDI/VDE 3516 Blatt 2:1981-07
|
Process analytical equipment for fluids |
VDI 3455:2013-08
|
Emission control - High-volume car body painting plants |
VDI 2083 Blatt 16.1:2010-08
|
Cleanroom technology - Barier systems (isolators, mini-environments, separative devices) - Effectiveness and certification |
DIN EN ISO 1135-3:2017-05
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
VDI 2083 Blatt 4.1:2006-10
|
Cleanroom technology - Planning, construction and start-up of cleanrooms |
VDI 2119:2013-06
|
Ambient air measurements - Sampling of atmospheric particles > 2,5 ?m on an acceptor surface using the Sigma-2 passive sampler - Characterisation by optical microscopy and calculation of number settling rate and mass concentration |
04/30098170 DC : DRAFT APR 2004
|
ISO 16232-10 - ROAD VEHICLES - FLUID CIRCUITS - CLEANLINESS OF COMPONENTS - PART 10: EXPRESSION OF RESULTS |
UNE-EN ISO 14644-14:2017
|
Cleanrooms and associated controlled environments - Part 14: Assessment of suitability for use of equipment by airborne particle concentration (ISO 14644-14:2016) |
BS ISO 20437:2017
|
Natural rubber latex cleanroom gloves. Specification |
EN ISO 15378:2017
|
Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) (ISO 15378:2017) |
ASTM F 2444 : 2004 : R2018
|
Standard Practice for Damage Prevention of Bearings, and Bearing Components Through Proper Handling Techniques |
16/30326493 DC : 0
|
BS EN ISO 14644-3 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 3: TEST METHODS |
BS ISO 16232-6:2007
|
Road vehicles. Cleanliness of components of fluid circuits Particle mass determination by gravimetric analysis |
15/30317874 DC : 0
|
BS EN 16844 - AESTHETIC MEDICINE SERVICES - NON-SURGICAL MEDICAL PROCEDURES |
14/30280736 DC : 0
|
BS EN ISO 14644-14 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 14 ASSESSMENT OF SUITABILITY FOR USE OF EQUIPMENT BY AIRBORNE PARTICLE CONCENTRATION |
07/30172614 DC : 0
|
BS ISO 18938 - IMAGING MATERIALS - OPTICAL DISCS - CARE AND HANDLING FOR EXTENDED STORAGE |
BS ISO 18913:2012
|
Imaging materials. Permanence. Vocabulary |
I.S. CEN ISO TR 14969:2005
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485: 2003 |
04/19987843 DC : DRAFT OCT 2004
|
BS ISO 13697 - OPTICS AND PHOTONICS - LASERS AND LASER-RELATED EQUIPMENT - TEST METHODS FOR SPECULAR REFLECTANCE AND TRANSMITTANCE OF OPTICAL LASER COMPONENTS |
10/30152881 DC : DRAFT DEC 2010
|
BS EN ISO 14644-2 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 2: SPECIFICATIONS FOR MONITORING AND PERIODIC TESTING TO PROVE CONTINUED COMPLIANCE WITH ISO 14644-1 |
UNI EN ISO 5667-23 : 2011
|
WATER QUALITY - SAMPLING - PART 23: GUIDANCE ON PASSIVE SAMPLING IN SURFACE WATERS |
13/30255929 DC : 0
|
BS EN ISO 7396-1 - MEDICAL GAS PIPELINE SYSTEMS - PART 1: PIPELINE SYSTEMS FOR COMPRESSED MEDICAL GASES AND VACUUM |
ASTM E 2311 : 2004 : R2009
|
Standard Practice for QCM Measurement of Spacecraft Molecular Contamination in Space |
BS ISO 15388:2012
|
Space systems. Contamination and cleanliness control |
BS PD ISO/TR 14969 : 2004 AMD 15958
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
04/30098096 DC : DRAFT APR 2004
|
ISO 16232-6 - ROAD VEHICLES - CLEANLINESS OF COMPONENTS OF FLUID CIRCUITS - PART 6: GRAVIMETRIC ANALYSIS |
DIN EN 16442 E : 2015
|
CONTROLLED ENVIRONMENT STORAGE CABINET FOR PROCESSED THERMOLABILE ENDOSCOPES |
ISO/IEC TS 22237-4:2018
|
Information technology Data centre facilities and infrastructures Part 4: Environmental control |
BS ISO 18385:2016
|
Minimizing the risk of human DNA contamination in products used to collect, store and analyze biological material for forensic purposes. Requirements |
16/30303345 DC : DRAFT JAN 2016
|
BS ISO 19724 - GASOLINE ENGINES WITH DIRECT INJECTION - CLEANLINESS ASSESSMENT OF FUEL INJECTION EQUIPMENT |
01/121101 DC : DRAFT MAR 2001
|
BS EN ISO 14644-7 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 7: SEPARATIVE ENCLOSURES (CLEAN AIR HOODS, GLOVEBOXES, ISOLATORS, MINI-ENVIRONMENTS) |
AAMI ISO TIR 14969 : 2004
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
BS ISO 4407:2002
|
Hydraulic fluid power. Fluid contamination. Determination of particulate contamination by the counting method using an optical microscope |
BS ISO 16232-4:2007
|
Road vehicles. Cleanliness of components of fluid circuits Method of extraction of contaminants by ultrasonic techniques |
ASTM F 1724 : 2001
|
Standard Test Method for Measuring Surface Metal Contamination of Polycrystalline Silicon by Acid Extraction-Atomic Absorption Spectroscopy (Withdrawn 2003) |
UNE-EN 16372:2015
|
Aesthetic surgery services |
12/30254927 DC : 0
|
BS EN 16372 - AESTHETIC SURGERY SERVICES |
DIN EN ISO 13408-2:2011-09
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 2: FILTRATION |
07/30090385 DC : 0
|
ISO 13408-1 - ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 1: GENERAL REQUIREMENTS |
BWB TL 6505-0488 : 1ED 2009
|
MEDICAL OXYGEN - 93% - GENERAL CONDITIONS |
AAMI ISO 13408-6 : 2005 : INC : AMD 1 : 2013
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 6: ISOLATOR SYSTEMS |
ASTM F 2444 : 2004 : R2012
|
Standard Practice for Damage Prevention of Bearings, and Bearing Components Through Proper Handling Techniques |
ISO 18385:2016
|
Minimizing the risk of human DNA contamination in products used to collect, store and analyze biological material for forensic purposes — Requirements |
I.S. EN 16372:2014
|
AESTHETIC SURGERY SERVICES |
ISO 11500:2008
|
Hydraulic fluid power — Determination of the particulate contamination level of a liquid sample by automatic particle counting using the light-extinction principle |
I.S. EN 16603-20-08:2014
|
SPACE ENGINEERING - PART 20-08: PHOTOVOLTAIC ASSEMBLIES AND COMPONENTS |
UNI EN ISO 13408-2 : 2011
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 2: FILTRATION |
ISO 21501-4:2007
|
Determination of particle size distribution Single particle light interaction methods Part 4: Light scattering airborne particle counter for clean spaces |
DIN EN ISO 7396-1:2016-09
|
MEDICAL GAS PIPELINE SYSTEMS - PART 1: PIPELINE SYSTEMS FOR COMPRESSED MEDICAL GASES AND VACUUM (ISO 7396-1:2016) |
ISO 16232-7:2007
|
Road vehicles Cleanliness of components of fluid circuits Part 7: Particle sizing and counting by microscopic analysis |
BS ISO 18413:2015
|
Hydraulic fluid power. Cleanliness of components. Inspection document and principles related to contaminant extraction and analysis, and data reporting |
ISO 16232-10:2007
|
Road vehicles Cleanliness of components of fluid circuits Part 10: Expression of results |
ASTM E 2088 : 2006 : R2015
|
Standard Practice for Selecting, Preparing, Exposing, and Analyzing Witness Surfaces for Measuring Particle Deposition in Cleanrooms and Associated Controlled Environments |
ASTM E 1549/E1549M : 2013 : R2016
|
Standard Specification for ESD Controlled Garments Required in Cleanrooms and Controlled Environments for Spacecraft for Non-Hazardous and Hazardous Operations |
ASTM F 25 : 2004
|
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Cleanrooms and Other Dust-Controlled Areas |
ISO/TR 14969:2004
|
Medical devices Quality management systems Guidance on the application of ISO 13485: 2003 |
ISO 11737-2:2009
|
Sterilization of medical devices Microbiological methods Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process |
ISO 17331:2004
|
Surface chemical analysis Chemical methods for the collection of elements from the surface of silicon-wafer working reference materials and their determination by total-reflection X-ray fluorescence (TXRF) spectroscopy |
EN 16844:2017
|
Aesthetic medicine services - Non-surgical medical treatments |
ISO 14706:2014
|
Surface chemical analysis Determination of surface elemental contamination on silicon wafers by total-reflection X-ray fluorescence (TXRF) spectroscopy |
BS EN ISO 11551:2003
|
Optics and optical instruments. Lasers and laser-related equipment. Test method for absorptance of optical laser components |
ISO 15388:2012
|
Space systems — Contamination and cleanliness control |
DIN EN ISO 14698-2 E : 2004
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL - PART 2: EVALUATION AND INTERPRETATION OF BIOCONTAMINATION DATA |
DIN EN ISO 14644-5:2005-03
|
Cleanrooms and associated controlled environments - Part 5: Operations (ISO 14644-5:2004) |
DIN EN ISO 14644-3:2006-03
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 3: TEST METHODS |
DIN EN ISO 14644-2:2016-05
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 2: MONITORING TO PROVIDE EVIDENCE OF CLEANROOM PERFORMANCE RELATED TO AIR CLEANLINESS BY PARTICLE CONCENTRATION (ISO 14644-2:2015) |
UNE-EN ISO 14644-2:2016
|
Cleanrooms and associated controlled environments - Part 2: Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration (ISO 14644-2:2015) |
ISO 1135-5:2015
|
Transfusion equipment for medical use — Part 5: Transfusion sets for single use with pressure infusion apparatus |
BS EN ISO 14698-2:2003
|
Cleanrooms and associated controlled environments. Biocontamination control Evaluation and interpretation of biocontamination data |
ISO 14644-5:2004
|
Cleanrooms and associated controlled environments — Part 5: Operations |
UNI EN ISO 8536-4 : 2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
BS EN ISO 1135-4:2015
|
Transfusion equipment for medical use Transfusion sets for single use, gravity feed |
NASA RPTSTD 8070 0001 : 2010 CHANGE 2 2013
|
SURFACE CLEANLINESS STANDARD OF FLUID SYSTEMS FOR ROCKET ENGINE TEST FACILITIES OF THE NASA ROCKET PROPULSION TEST PROGRAM |
NASA KSC C 123 : 2009
|
SURFACE CLEANLINESS OF GROUND SUPPORT EQUIPMENT FLUID SYSTEMS, SPECIFICATION FOR |
EN ISO 14698-2:2003/AC:2006
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL - PART 2: EVALUATION AND INTERPRETATION OF BIOCONTAMINATION DATA |
I.S. EN ISO 11737-2:2009
|
STERILIZATION OF MEDICAL DEVICES - MICROBIOLOGICAL METHODS - PART 2: TESTS OF STERILITY PERFORMED IN THE DEFINITION, VALIDATION AND MAINTENANCE OF A STERILIZATION PROCESS |
I.S. EN ISO 9073-10:2005
|
TEXTILES - TEST METHODS FOR NONWOVENS - PART 10: LINT AND OTHER PARTICLES GENERATION IN THE DRY STATE |
NASA MSFC STD 246 : 2011
|
STANDARD DESIGN AND OPERATIONAL CRITERIA FOR CONTROLLED ENVIRONMENTAL AREAS |
I.S. EN ISO 14698-2:2003
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL - PART 2: EVALUATION AND INTERPRETATION OF BIOCONTAMINATION DATA |
NASA PRC 5001 : 2011
|
PROCESS SPECIFICATION FOR CLEANING OF HARDWARE |
EN ISO 14698-1 : 2003
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL - PART 1: GENERAL PRINCIPLES AND METHODS |
EN ISO 29701 : 2010
|
Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010) |
EN ISO 14644-2:2015
|
Cleanrooms and associated controlled environments - Part 2: Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration (ISO 14644-2:2015) |
EN 16602-70-55:2015
|
Space product assurance - Microbiological examination of flight hardware and cleanrooms |
I.S. EN ISO 13696:2002
|
OPTICS AND OPTICAL INSTRUMENTS - TEST METHODS FOR RADIATION SCATTERED BY OPTICAL COMPONENTS |
DIN EN ISO 14644-13 E : 2017
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 13: CLEANING OF SURFACES TO ACHIEVE DEFINED LEVELS OF CLEANLINESS IN TERMS OF PARTICLE AND CHEMICAL CLASSIFICATIONS (ISO 14644-13:2017) |
ISO 12345:2013
|
Diesel engines Cleanliness assessment of fuel injection equipment |
05/30142385 DC : DRAFT NOV 2005
|
ISO 14644-6 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 6: VOCABULARY |
17/30319520 DC : 0
|
BS ISO 20289 - SURFACE CHEMICAL ANALYSIS - TOTAL REFLECTION X-RAY FLUORESCENCE ANALYSIS OF WATER SAMPLES |
02/122627 DC : DRAFT JULY 2002
|
BS ISO 17331 - SURFACE CHEMICAL ANALYSIS - CHEMICAL METHODS FOR THE COLLECTION OF ELEMENTS FROM THE SURFACE OF SILICON-WAFER WORKING-REFERENCE MATERIALS AND THEIR DETERMINATION BY TOTAL-REFLECTION X-RAY FLUORESCENCE SPECTROSCOPY (TXRF) |
I.S. EN 14091:2002
|
SPACE PRODUCT ASSURANCE - THERMAL VACUUM OUTGASSING TEST FOR THE SCREENING OF SPACE MATERIALS |
I.S. EN ISO 29701:2010
|
NANOTECHNOLOGIES - ENDOTOXIN TEST ON NANOMATERIAL SAMPLES FOR IN VITRO SYSTEMS - LIMULUS AMEBOCYTE LYSATE (LAL) TEST |
MIL-PRF-38535 Revision K:2013
|
Integrated Circuits (Microcircuits) Manufacturing, General Specification for |
11/30205822 DC : 0
|
BS ISO 18913 - IMAGING MATERIALS - PERMANENCE - VOCABULARY |
AAMI ISO TIR 17665-2 : 2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ANSI/AAMI/ISO 17665-1 |
16/30299911 DC : 0
|
BS ISO 21501-4 - DETERMINATION OF PARTICLE SIZE DISTRIBUTION - SINGLE PARTICLE LIGHT INTERACTION METHODS - PART 4: LIGHT SCATTERING AIRBORNE PARTICLE COUNTER FOR CLEAN SPACES |
I.S. EN 14777:2004
|
SPACE ENGINEERING - MULTIPACTION DESIGN AND TEST |
BS EN ISO 29701:2010
|
Nanotechnologies. Endotoxin test on nanomaterial samples for in vitro systems. Limulus amebocyte lysate (LAL) test |
BS ISO 11040-4:2015
|
Prefilled syringes Glass barrels for injectables and sterilized subassembled syringes ready for filling |
DIN EN ISO 24998:2009-03
|
PLASTICS LABORATORY WARE - SINGLE-USE PETRI DISHES FOR MICROBIOLOGICAL PROCEDURES |
DIN EN ISO 1135-3 E : 2017
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
BS ISO 12345:2013
|
Diesel engines. Cleanliness assessment of fuel injection equipment |
13/30273499 DC : 0
|
BS ISO 11040-4 - PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING |
ARP1176A : 2013(R2018)
|
OXYGEN SYSTEM AND COMPONENT CLEANING |
BS ISO 11500:2008
|
Hydraulic fluid power. Determination of the particulate contamination level of a liquid sample by automatic particle counting using the light-extinction principle |
17/30302489 DC : DRAFT MAR 2017
|
BS EN ISO 13408-2 - ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 2: STERILIZING FILTRATION |
05/30105136 DC : DRAFT APR 2005
|
ISO 24013 - OPTICS AND PHOTONICS - LASERS AND LASER RELATED EQUIPMENT - MEASUREMENT OF OPTICAL PHASE SHIFT OF OPTICAL COMPONENTS |
EN ISO 13408-6:2011/A1:2013
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 6: ISOLATOR SYSTEMS (ISO 13408-6:2005/AMD 1:2013) |
UNE-EN ISO 13408-2:2011
|
Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003) |
16/30348371 DC : 0
|
BS ISO 14644-12 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 12: SPECIFICATIONS FOR MONITORING AIR CLEANLINESS BY NANOSCALE PARTICLE CONCENTRATION |
08/30190157 DC : DRAFT SEP 2008
|
BS EN ISO 14644-9 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 9: CLASSIFICATION OF SURFACE PARTICLE CLEANLINESS |
03/314215 DC : DRAFT OCT 2003
|
ISO TR 14969 - MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
14/30289934 DC : 0
|
BS ISO 18385 - MINIMIZING THE RISK OF DNA CONTAMINATION IN PRODUCTS USED TO COLLECT AND ANALYSE BIOLOGICAL MATERIAL FOR FORENSIC PURPOSES |
13/30281524 DC : 0
|
BS ISO 18938 - IMAGING MATERIALS - OPTICAL DISCS - CARE AND HANDLING FOR EXTENDED STORAGE |
10/30234886 DC : 0
|
BS ISO 15388 - SPACE SYSTEMS - CONTAMINATION AND CLEANLINESS CONTROL |
01/122934 DC : DRAFT AUG 2001
|
BS EN ISO 14644-5 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 5: OPERATIONS |
UNI EN ISO 14644-10 : 2013
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 10: CLASSIFICATION OF SURFACE CLEANLINESS BY CHEMICAL CONCENTRATION |
I.S. EN 16602-70-08:2015
|
SPACE PRODUCT ASSURANCE - MANUAL SOLDERING OF HIGH-RELIABILITY ELECTRICAL CONNECTIONS |
07/30163423 DC : 0
|
BS ISO 24998 - PLASTICS LABORATORY WARE - SINGLE USE PETRI DISHES FOR MICROBIOLOGICAL PROCEDURES |
BS ISO 14706:2014
|
Surface chemical analysis. Determination of surface elemental contamination on silicon wafers by total-reflection X-ray fluorescence (TXRF) spectroscopy |
09/30175345 DC : 0
|
BS ISO 29701 - NANOTECHNOLOGIES - ENDOTOXIN TEST ON NANOMATERIAL SAMPLES FOR IN VITRO SYSTEMS - LIMULUS AMEBOCYTE LYSATE (LAL) TEST |
17/30311287 DC : 0
|
BS ISO 19924 - SPACE SYSTEMS - ACOUSTIC TESTING |
00/705381 DC : DRAFT FEB 2000
|
ISO/CD 15388 - SPACE SYSTEMS - CONTAMINATION AND CLEANLINESS CONTROL |
BS ISO 16232-2:2007
|
Road vehicles. Cleanliness of components of fluid circuits Method of extraction of contaminants by agitation |
AAMI ST67 : 2011 : R2017
|
STERILIZATION OF HEALTH CARE PRODUCTS - REQUIREMENTS AND GUIDANCE FOR SELECTING A STERILITY ASSURANCE LEVEL (SAL) FOR PRODUCTS LABELED 'STERILE' |
02/564513 DC : DRAFT OCT 2002
|
BS EN ISO 1135-4 - INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE |
CSA ISO TR 14969 : 2005 : R2015
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
AAMI TIR52 : 2014
|
ENVIRONMENTAL MONITORING FOR TERMINALLY STERILIZED HEALTHCARE PRODUCTS |
AAMI ISO 13408-1 : 2008 : INC : AMD 1 : 2013 : R201100
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 1: GENERAL REQUIREMENTS |
01/560508 DC : DRAFT FEB 2001
|
BS ISO 13408-2 - ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 2: FILTRATION |
AAMI ISO 13408-6:2005
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 6: ISOLATOR SYSTEMS |
DIN EN 16442:2015-05
|
CONTROLLED ENVIRONMENT STORAGE CABINET FOR PROCESSED THERMOLABILE ENDOSCOPES |
AAMI ISO 13408-1:2008
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 1: GENERAL REQUIREMENTS |
PREN 17141 : DRAFT 2017
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL |
CSA ISO TR 14969 :2005
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
ANSI/AAMI/ISO 13408-6:2005(R2013)&A1:2013
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 6: ISOLATOR SYSTEMS |
I.S. EN ISO 14644-13:2017
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 13: CLEANING OF SURFACES TO ACHIEVE DEFINED LEVELS OF CLEANLINESS IN TERMS OF PARTICLE AND CHEMICAL CLASSIFICATIONS (ISO 14644-13:2017) |
UNE-EN 16442:2015
|
Controlled environment storage cabinet for processed thermolabile endoscopes |
BS ISO 17331 : 2004
|
SURFACE CHEMICAL ANALYSIS - CHEMICAL METHODS FOR THE COLLECTION OF ELEMENTS FROM THE SURFACE OF SILICON-WAFER WORKING REFERENCE MATERIALS AND THEIR DETERMINATION BY TOTAL-REFLECTION X-RAY FLUORESCENCE (TXRF) SPECTROSCOPY |
AAMI/ISO TIR17665-2:2009(R2016)
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ANSI/AAMI/ISO 17665-1 |
I.S. EN ISO 1135-3:2017
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
ISO 16232-2:2007
|
Road vehicles Cleanliness of components of fluid circuits Part 2: Method of extraction of contaminants by agitation |
ISO 20437:2017
|
Natural rubber latex cleanroom gloves — Specification |
S.R. CEN/TS 16244:2018
|
VENTILATION IN HOSPITALS - COHERENT HIERARCHIC STRUCTURE AND COMMON TERMS AND DEFINITIONS FOR A STANDARD RELATED TO VENTILATION IN HOSPITALS |
ASTM F 3218 : 2017
|
Standard Practice for Recording Environmental Effects for Utilization with A-UGV Test Methods |
ASTM E 2042/E2042M : 2009 : R2016
|
Standard Practice for Cleaning and Maintaining Controlled Areas and Clean Rooms |
ASTM F 2332 : 2006 : R2013
|
Standard Specification for Annular Ball Bearings for Instruments and Precision Rotating Components |
ASTM E 1235 : 2012 : REDLINE
|
Standard Test Method for Gravimetric Determination of Nonvolatile Residue (NVR) in Environmentally Controlled Areas for Spacecraft |
ASTM F 25/F25M : 2009
|
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Cleanrooms and Other Dust-Controlled Areas |
ASTM G 93 : 2003 : EDT 1
|
Standard Practice for Cleaning Methods and Cleanliness Levels for Material and Equipment Used in Oxygen-Enriched Environments |
UNE-EN ISO 7396-1:2016
|
Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2016) |
I.S. EN ISO 11551:2004
|
OPTICS AND OPTICAL INSTRUMENTS - LASERS AND LASER-RELATED EQUIPMENT - TEST METHOD FOR ABSORPTANCE OF OPTICAL LASER COMPONENTS |
I.S. EN ISO 24998:2008
|
PLASTICS LABORATORY WARE - SINGLE-USE PETRI DISHES FOR MICROBIOLOGICAL PROCEDURES |
ISO/TR 18196:2016
|
Nanotechnologies — Measurement technique matrix for the characterization of nano-objects |
ISO 18938:2014
|
Imaging materials — Optical discs — Care and handling for extended storage |
ISO 7396-1:2016
|
Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum |
ISO 11040-4:2015
|
Prefilled syringes Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling |
I.S. EN ISO 13408-1:2015
|
ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 1: GENERAL REQUIREMENTS (ISO 13408-1:2008, INCLUDING AMD 1:2013) |
IEC TR 62258-3:2010
|
Semiconductor die products - Part 3: Recommendations for good practice in handling, packing and storage |
I.S. EN ISO 8536-4:2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010) |
BS EN ISO 8536-4 : 2013
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED |
DIN EN ISO 8536-4:2013-07
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010 + AMD 1:2013) |
UNE-EN ISO 1135-4:2016
|
Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed (ISO 1135-4:2015) |
ISO 14644-2:2015
|
Cleanrooms and associated controlled environments Part 2: Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration |
ISO 11551:2003
|
Optics and optical instruments Lasers and laser-related equipment Test method for absorptance of optical laser components |
BS EN ISO 14644-5:2004
|
Cleanrooms and associated controlled environments Operations |
ISO 1135-3:2016
|
Transfusion equipment for medical use Part 3: Blood-taking sets for single use |
ISO/TS 80004-6:2013
|
Nanotechnologies Vocabulary Part 6: Nano-object characterization |
ISO 13696:2002
|
Optics and optical instruments Test methods for radiation scattered by optical components |
ISO 14644-4:2001
|
Cleanrooms and associated controlled environments — Part 4: Design, construction and start-up |
ISO 14644-14:2016
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Cleanrooms and associated controlled environments Part 14: Assessment of suitability for use of equipment by airborne particle concentration |
EN ISO 11737-2:2009
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Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009) |
BS EN 131-2 : 2010
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LADDERS - PART 2: REQUIREMENTS, TESTING, MARKING |
BS EN ISO 14644-3:2005
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Cleanrooms and associated controlled environments Test methods |
BS EN ISO 13696:2002
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Optics and optical instruments. Test methods for radiation scattered by optical components |
ISO 1135-4:2015
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Transfusion equipment for medical use — Part 4: Transfusion sets for single use, gravity feed |
ISO 14698-1:2003
|
Cleanrooms and associated controlled environments Biocontamination control Part 1: General principles and methods |
ISO 8536-4:2010
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Infusion equipment for medical use Part 4: Infusion sets for single use, gravity feed |
BS EN ISO 14644-7:2004
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Cleanrooms and associated controlled environments Separative devices (clean air hoods, gloveboxes, isolators and mini-environments) |
I.S. EN ISO 14644-2:2015
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CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 2: MONITORING TO PROVIDE EVIDENCE OF CLEANROOM PERFORMANCE RELATED TO AIR CLEANLINESS BY PARTICLE CONCENTRATION (ISO 14644-2:2015) |
ISO 13697:2006
|
Optics and photonics Lasers and laser-related equipment Test methods for specular reflectance and regular transmittance of optical laser components |
BS EN ISO 24013:2006
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Optics and photonics. Lasers and laser-related equipment. Measurement of phase retardation of optical components for polarized laser radiation |
ISO 9073-10:2003
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Textiles Test methods for nonwovens Part 10: Lint and other particles generation in the dry state |
EN ISO 24013:2006
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Optics and photonics - Lasers and laser-related equipment - Measurement of phase retardation of optical components for polarized laser radiation (ISO 24013:2006) |
EN 14777:2004
|
Space engineering - Multipaction design and test |
EN 16372:2014
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Aesthetic surgery services |
EN ISO 1135-3:2017
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Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016) |
EN ISO 11551:2003
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Optics and optical instruments - Lasers and laser-related equipment - Test method for absorptance of optical laser components (ISO 11551:2003) |
EN ISO 14644-5:2004
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Cleanrooms and associated controlled environments - Part 5: Operations (ISO 14644-5:2004) |
EN ISO 5667-23:2011
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Water quality - Sampling - Part 23: Guidance on passive sampling in surface waters (ISO 5667-23:2011) |
EN ISO 13408-1:2015
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Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013) |
EN ISO 14644-10:2013
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Cleanrooms and associated controlled environments - Part 10: Classification of surface cleanliness by chemical concentration (ISO 14644-10:2013) |
EN ISO 24998:2008
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Plastics laboratory ware - Single-use Petri dishes for microbiological procedures (ISO 24998:2008) |
EN 16602-70-58:2015
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Space product assurance - Bioburden control of cleanrooms |
EN ISO 14644-6:2007
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CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 6: VOCABULARY |
EN ISO 14644-4:2001
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Cleanrooms and associated controlled environments - Part 4: Design, construction and start-up (ISO 14644-4:2001) |
EN ISO 14644-14:2016
|
Cleanrooms and associated controlled environments - Part 14: Assessment of suitability for use of equipment by airborne particle concentration (ISO 14644-14:2016) |
EN 14091:2002
|
Space product assurance - Thermal vacuum outgassing test for the screening of space materials |
EN ISO 13696:2002
|
Optics and optical instruments - Test methods for radiation scattered by optical components (ISO 13696:2002) |
EN ISO 13697:2006
|
Optics and photonics - Lasers and laser-related equipment - Test methods for specular reflectance and regular transmittance of optical laser components (ISO 13697:2006) |
EN ISO 1135-5:2015
|
Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015) |
EN ISO 14644-3:2005
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CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 3: TEST METHODS |
EN 13824 : 2004
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STERILIZATION OF MEDICAL DEVICES - ASEPTIC PROCESSING OF LIQUID MEDICAL DEVICES - REQUIREMENTS |
EN ISO 9073-10:2004
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Textiles - Test methods for nonwovens - Part 10: Lint and other particles generation in the dry state (ISO 9073-10:2003) |
EN 16603-20-08:2014
|
Space engineering - Part 20-08: Photovoltaic assemblies and components |
EN 16442:2015
|
Controlled environment storage cabinet for processed thermolabile endoscopes |
EN 16602-70-08:2015
|
Space product assurance - Manual soldering of high-reliability electrical connections |
DIN ISO 10083:2008-12
|
OXYGEN CONCENTRATOR SUPPLY SYSTEMS FOR USE WITH MEDICAL GAS PIPELINE SYSTEMS |
EN ISO 14644-15:2017
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Cleanrooms and associated controlled environments - Part 15: Assessment of suitability for use of equipment and materials by airborne chemical concentration (ISO 14644-15:2017) |
13/30261893 DC : 0
|
BS EN ISO 14644-12 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 12: CLASSIFICATION OF AIR CLEANLINESS BY NANOSCALE PARTICLE CONCENTRATION |
BS EN ISO 5667-23:2011
|
Water quality. Sampling Guidance on passive sampling in surface waters |
BS PD IEC TR 62258-3 : 2005
|
SEMICONDUCTOR DIE PRODUCTS - PART 3: RECOMMENDATIONS FOR GOOD PRACTICE IN HANDLING, PACKING AND STORAGE |
MIL-STD-648 Revision E:2016
|
Specialized Shipping Containers |
BS ISO 19724:2016
|
Gasoline engines with direct injection. Cleanliness assessment of fuel injection equipment |
UNE-EN ISO 14644-10:2014
|
Cleanrooms and associated controlled environments - Part 10: Classification of surface cleanliness by chemical concentration (ISO 14644-10:2013) |
BS EN 16372:2014
|
Aesthetic surgery services |
BS EN ISO 1135-5:2015
|
Transfusion equipment for medical use Transfusion sets for single use with pressure infusion apparatus |
MIL-STD-750-5 Base Document:2012
|
HIGH RELIABILITY SPACE APPLICATION TEST METHODS FOR SEMICONDUCTOR DEVICES - PART 5: TEST METHODS 5000 THROUGH 5999 |
BS EN ISO 1135-3:2017
|
Transfusion equipment for medical use Blood-taking sets for single use |
AES 49 : 2005(R2010)
|
|
BS ISO 16232-1:2007
|
Road vehicles. Cleanliness of components of fluid circuits Vocabulary |
DIN EN ISO 5667-23 E : 2011
|
WATER QUALITY - SAMPLING - PART 23: GUIDANCE ON PASSIVE SAMPLING IN SURFACE WATERS |
I.S. EN ISO 7396-1:2016
|
MEDICAL GAS PIPELINE SYSTEMS - PART 1: PIPELINE SYSTEMS FOR COMPRESSED MEDICAL GASES AND VACUUM (ISO 7396-1:2016) |
DIN 50451-2:2003-04
|
Determination of trace elements in liquids for use in semiconductor technology - Part 2: Determination of calcium, chromium, cobalt, copper, iron, nickel and zinc in hydrofluoric acid by plasma emission spectroscopy |
DIN EN ISO 1135-3:2014-12 (Draft)
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
DD CEN ISO/TS 17665-2:2009
|
Sterilization of health care products. Moist heat Guidance on the application of ISO 17665-1 |
PD CEN ISO/TR 14969:2005
|
Medical devices. Quality management systems. Guidance on the application of ISO 13485:2003 |
MIL-PRF-38534 Revision K:2017
|
HYBRID MICROCIRCUITS, GENERAL SPECIFICATION FOR |
CSA Z17665-2 : 2009 : R2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ISO 17665-1 |
S.R. CEN ISO/TS 17665-2:2009
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - PART 2: GUIDANCE ON THE APPLICATION OF ISO 17665-1 |
DIN ISO 11040-4:2007-10
|
PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015) |
BS IEC 61340-5.1 : 1998 AMD 13198
|
ELECTROSTATICS - PART 5-1: PROTECTION OF ELECTRONIC DEVICES FROM ELECTROSTATIC PHENOMENA - GENERAL REQUIREMENTS |
13/30283694 DC : 0
|
BS EN ISO 1135-5 - TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS |
BS EN ISO 14644-14:2016
|
ENISO 14644-14 environments — Assessment of suitability of equipment and materials for cleanrooms Assessment of suitability for use of equipment by airborne particle concentration |
04/30079743 DC : DRAFT APR 2004
|
ISO 15378 - PRIMARY PACKAGING MATERIALS FOR MEDICINAL PRODUCTS - PARTICULAR REQUIREMENTS FOR THE APPLICATION OF ISO 9001:2000 WITH REFERENCE TO GOOD MANUFACTURING PRACTICE (GMP) |
17/30329441 DC : 0
|
BS EN 17141 - CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - BIOCONTAMINATION CONTROL |
CSA Z10083 : 2008 : R2013
|
OXYGEN CONCENTRATOR SUPPLY SYSTEMS FOR USE WITH MEDICAL GAS PIPELINE SYSTEMS |
CSA ISO TR 14969 : 2005 : R2010
|
MEDICAL DEVICES - QUALITY MANAGEMENT SYSTEMS - GUIDANCE ON THE APPLICATION OF ISO 13485:2003 |
04/30098083 DC : DRAFT APR 2004
|
ISO 16232-2 - ROAD VEHICLES - FLUID CIRCUITS - CLEANLINESS OF COMPONENTS - PART 2: METHOD OF EXTRACTION OF CONTAMINANTS BY AGITATION |
AAMI ISO TIR 17665-3:2014
|
STERILIZATION OF HEALTH CARE PRODUCTS - MOIST HEAT - GUIDANCE ON THE DESIGNATION OF A MEDICAL PRODUCT TO A PRODUCT FAMILY AND PROCESSING CATEGORY FOR STEAM STERILIZATION |
ISO 14644-13:2017
|
Cleanrooms and associated controlled environments — Part 13: Cleaning of surfaces to achieve defined levels of cleanliness in terms of particle and chemical classifications |
CSA Z5100/Z5200 PACKAGE : 2017
|
CONSISTS OF Z5100-17, CELLULOSE NANOMATERIALS - TEST METHODS FOR CHARACTERIZATION AND Z5200-17, CELLULOSE NANOMATERIALS - BLANK DETAIL SPECIFICATION |
ASTM E 1234 : 2012 : REDLINE
|
Standard Practice for Handling, Transporting, and Installing Nonvolatile Residue (NVR) Sample Plates Used in Environmentally Controlled Areas for Spacecraft |
ISO 24998:2008
|
Plastics laboratory ware — Single-use Petri dishes for microbiological procedures |
UNE 171340:2012
|
Validation and evaluation of controlled environment rooms in hospitals |
CEN/TS 16244:2018
|
Ventilation in hospitals - Coherent hierarchic structure and common terms and definitions for a standard related to ventilation in hospitals |
ASTM E 2614 : 2015 : REDLINE
|
Standard Guide for Evaluation of Cleanroom Disinfectants |
ISO 14644-15:2017
|
Cleanrooms and associated controlled environments — Part 15: Assessment of suitability for use of equipment and materials by airborne chemical concentration |
CEI CLC/TR 62258-3 : 2007
|
SEMICONDUCTOR DIE PRODUCTS - PART 3: RECOMMENDATIONS FOR GOOD PRACTICE IN HANDLING, PACKING AND STORAGE |
ISO/TS 17665-3:2013
|
Sterilization of health care products — Moist heat — Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization |
16/30341759 DC : 0
|
BS EN 16602-70-54 - SPACE PRODUCT ASSURANCE - ULTRACLEANING OF FLIGHT HARDWARE |
UNI EN ISO 24998 : 2009
|
PLASTICS LABORATORY WARE - SINGLE-USE PETRI DISHES FOR MICROBIOLOGICAL PROCEDURES |
PD CEN/TS 16244:2018
|
Ventilation in hospitals. Coherent hierarchic structure and common terms and definitions for a standard related to ventilation in hospitals |
ASTM F 50 : 2012
|
Standard Practice for Continuous Sizing and Counting of Airborne Particles in Dust-Controlled Areas and Clean Rooms Using Instruments Capable of Detecting Single Sub-Micrometre and Larger Particles |
ASTM A 380/A380M : 2017
|
Standard Practice for Cleaning, Descaling, and Passivation of Stainless Steel Parts, Equipment, and Systems |
ASTM E 2352 : 2004 : R2010
|
Standard Practice for Aerospace Cleanrooms and Associated Controlled Environments-Cleanroom Operations |
ISO 16232-3:2007
|
Road vehicles Cleanliness of components of fluid circuits Part 3: Method of extraction of contaminants by pressure rinsing |
BS EN 16844 : 2017
|
AESTHETIC MEDICINE SERVICES - NON-SURGICAL MEDICAL TREATMENTS |
ISO 18413:2015
|
Hydraulic fluid power Cleanliness of components Inspection document and principles related to contaminant extraction and analysis, and data reporting |
ISO 16232-4:2007
|
Road vehicles Cleanliness of components of fluid circuits Part 4: Method of extraction of contaminants by ultrasonic techniques |
ASTM F 25/F25M : 2009 : R2015
|
Standard Test Method for Sizing and Counting Airborne Particulate Contamination in Cleanrooms and Other Dust-Controlled Areas |
ISO 16232-6:2007
|
Road vehicles Cleanliness of components of fluid circuits Part 6: Particle mass determination by gravimetric analysis |
I.S. EN ISO 15378:2017
|
PRIMARY PACKAGING MATERIALS FOR MEDICINAL PRODUCTS - PARTICULAR REQUIREMENTS FOR THE APPLICATION OF ISO 9001:2015, WITH REFERENCE TO GOOD MANUFACTURING PRACTICE (GMP) (ISO 15378:2017) |
ONORM EN ISO 14644-3 : 2006
|
CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 3: TEST METHODS |
DIN EN ISO 9073-10 E : 2005
|
TEXTILES - TEST METHODS FOR NONWOVENS - PART 10: LINT AND OTHER PARTICLES GENERATION IN THE DRY STATE |
DIN EN ISO 11737-2:2010-04
|
STERILIZATION OF MEDICAL DEVICES - MICROBIOLOGICAL METHODS - PART 2: TESTS OF STERILITY PERFORMED IN THE DEFINITION, VALIDATION AND MAINTENANCE OF A STERILIZATION PROCESS |
UNE-EN ISO 11737-2:2010
|
Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009) |
IEC 62258-1:2009
|
Semiconductor die products - Part 1: Procurement and use |
ISO 5667-23:2011
|
Water quality Sampling Part 23: Guidance on passive sampling in surface waters |
ISO 14698-2:2003
|
Cleanrooms and associated controlled environments Biocontamination control Part 2: Evaluation and interpretation of biocontamination data |
BS EN 14091:2002
|
Space product assurance. Thermal vacuum outgassing test for the screening of space materials |
BS EN ISO 8871-3:2004
|
Elastomeric parts for parenterals and for devices for pharmaceuticals use Determination of released-particle count |
BS EN 14777:2004
|
Space engineering. Multipaction design and test |
ISO 29701:2010
|
Nanotechnologies Endotoxin test on nanomaterial samples for in vitro systems Limulus amebocyte lysate (LAL) test |
ISO 24013:2006
|
Optics and photonics — Lasers and laser-related equipment — Measurement of phase retardation of optical components for polarized laser radiation |
ISO/TS 17665-2:2009
|
Sterilization of health care products — Moist heat — Part 2: Guidance on the application of ISO 17665-1 |
CEI EN 62258-1 : 2011
|
SEMICONDUCTOR DIE PRODUCTS - PART 1: PROCUREMENT AND USE |
EN ISO 1135-4 : 2015 COR 2016
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015) |
DIN EN ISO 14698-2:2004-02
|
Cleanrooms and associated controlled environments - Biocontamination control - Part 2: Evaluation and interpretation of biocontamination data (ISO 14698-2:2003) |
DIN EN ISO 9073-10:2005-03
|
TEXTILES - TEST METHODS FOR NONWOVENS - PART 10: LINT AND OTHER PARTICLES GENERATION IN THE DRY STATE |
DIN EN ISO 5667-23:2011-06
|
Water quality - Sampling - Part 23: Guidance on passive sampling in surface waters (ISO 5667-23:2011) |
DIN EN 13824:2005-02
|
STERILIZATION OF MEDICAL DEVICES - ASEPTIC PROCESSING OF LIQUID MEDICAL DEVICES - REQUIREMENTS |
DIN EN ISO 13697:2006-08
|
Optics and photonics - Lasers and laser-related equipment - Test methods for specular reflectance and regular transmittance of optical laser components (ISO 13697:2006) |
EN 131-2:2010+A2:2017
|
Ladders - Part 2: Requirements, testing, marking |
DIN ISO 11040-4:2017-07
|
PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015) |
DIN EN ISO 14644-7:2005-01
|
Cleanrooms and associated controlled environments - Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments) (ISO 14644-7:2004); German version EN ISO 14644-7:2004 |
CEN ISO/TS 17665-2:2009
|
Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO/TS 17665-2:2009) |