DIN EN ISO 29701:2011-01
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Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010) |
17/30354017 DC : 0
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BS ISO 16232 - ROAD VEHICLES - CLEANLINESS OF COMPONENTS AND SYSTEMS |
DIN EN ISO 1135-5:2016-06
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TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 5: TRANSFUSION SETS FOR SINGLE USE WITH PRESSURE INFUSION APPARATUS (ISO 1135-5:2015) |
DIN EN ISO 13408-6:2013-07
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Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005 + Amd 1:2013) (includes Amendment A1:2013) |
DIN HDBK 406 : 2ED 2016
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DIN EN ISO 13408-1:2015-12
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ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 1: GENERAL REQUIREMENTS (ISO 13408-1:2008, INCLUDING AMD 1:2013) |
DIN 50451-1:2003-04
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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 EN ISO 14644-10:2013-06
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Cleanrooms and associated controlled environments - Part 10: Classification of surface cleanliness by chemical concentration (ISO 14644-10:2013) |
DIN EN ISO 1135-4:2016-06
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TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015) |
DIN EN ISO 24013:2007-02
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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) |
VDI 2083 Blatt 17:2013-06
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Cleanroom technology - Compatibility of materials with the required cleanliness |
VDI 2083 Blatt 18:2012-01
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Cleanroom technology - Biocontamination control |
VDI 2083 Blatt 3.1:2012-06
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Cleanroom technology - Metrology in cleanroom air - Monitoring |
VDI 2083 Blatt 15:2007-04
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Cleanroom technology - Personnel at the clean work place |
VDI 4066 Blatt 1:2013-05
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Hygienic requirements for the production and aseptically filling of beverage products - Principles and design criteria |
VDI 6305:2016-12 (Draft)
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Technical good manufacturing practice - Application guideline for projects in the GMP environment |
VDI 2083 Blatt 8.1:2014-10
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Cleanroom technology - Air cleanliness chemical concentration (ACC) |
VDI 2083 Blatt 9.2:2017-01
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Cleanroom technology - Consumables in the cleanroom |
VDI 2083 Blatt 16.2:2015-10 (Draft)
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Cleanroom technology - Barrier systems - Mini-environments |
VDI 2083 Blatt 1:2013-01
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Cleanroom technology - Particulate air cleanliness classes |
VDI 2083 Blatt 3:2005-07
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Cleanroom technology - Metrology and test methods |
VDI/VDE 2627 Blatt 1:2015-12
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Measuring rooms - Classification and characteristics - Planning and execution |
VDI 2083 Blatt 13.2:2009-01
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Cleanroom technology - Quality, production and distribution of ultrapure water - Microelectronics and other technical applications |
VDI 2083 Blatt 13.1:2009-01
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Cleanroom technology - Quality, production and distribution of ultrapure water - Fundamentals |
VDI/VDE 3516 Blatt 2:1981-07
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Process analytical equipment for fluids |
VDI 3455:2013-08
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Emission control - High-volume car body painting plants |
VDI 2083 Blatt 16.1:2010-08
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Cleanroom technology - Barier systems (isolators, mini-environments, separative devices) - Effectiveness and certification |
VDI 2119:2013-06
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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 |
DIN EN ISO 13408-2:2011-09
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ASEPTIC PROCESSING OF HEALTH CARE PRODUCTS - PART 2: FILTRATION |
DIN EN ISO 7396-1:2016-09
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MEDICAL GAS PIPELINE SYSTEMS - PART 1: PIPELINE SYSTEMS FOR COMPRESSED MEDICAL GASES AND VACUUM (ISO 7396-1:2016) |
DIN EN ISO 14644-3:2006-03
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CLEANROOMS AND ASSOCIATED CONTROLLED ENVIRONMENTS - PART 3: TEST METHODS |
DIN EN ISO 1135-3:2014-12 (Draft)
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TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 3: BLOOD-TAKING SETS FOR SINGLE USE (ISO 1135-3:2016) |
DIN EN ISO 8536-4:2013-07
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INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010 + AMD 1:2013) |
DIN ISO 10083:2008-12
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OXYGEN CONCENTRATOR SUPPLY SYSTEMS FOR USE WITH MEDICAL GAS PIPELINE SYSTEMS |
DIN 50451-2:2003-04
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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 ISO 11040-4:2007-10
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PREFILLED SYRINGES - PART 4: GLASS BARRELS FOR INJECTABLES AND STERILIZED SUBASSEMBLED SYRINGES READY FOR FILLING (ISO 11040-4:2015) |
DIN EN ISO 80601-2-69:2014-12
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Medical electrical equipment - Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment (ISO 80601-2-69:2014) |
DIN EN ISO 11737-2:2010-04
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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 |