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SEMI E45 : NOV 2001(R2007)
|
TEST METHOD FOR THE DETERMINATION OF INORGANIC CONTAMINATION FROM MINIENVIRONMENTS USING VAPOR PHASE DECOMPOSITION-TOTAL REFLECTION X-RAY SPECTROSCOPY (VPD-TXRF) AND VAPOR PHASE DECOMPOSITION-ATOMIC ABSORPTION SPECTROSCOPY (VPD/ICP-MS) |
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SEMI E46 : 2007
|
TEST METHOD FOR THE DETERMINATION OF ORGANIC CONTAMINATION FROM MINIENVIRONMENTS USING ION MOBILITY SPECTROMETRY (IMS) |
|
EN 12298:1998
|
Biotechnology - Equipment - Guidance on testing procedures for leaktightness |
|
ISO 10648-1:1997
|
Containment enclosures — Part 1: Design principles |
|
SEMI S11 : 1996
|
ENVIRONMENTAL SAFETY, AND HEALTH GUIDELINES FOR SEMICONDUCTOR MANUFACTURING EQUIPMENT MINIENVIRONMENTS |
|
ISO 14698-2:2003
|
Cleanrooms and associated controlled environments Biocontamination control Part 2: Evaluation and interpretation of biocontamination data |
|
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 |
|
SEMI E19 : APR 2017
|
SPECIFICATION FOR STANDARD MECHANICAL INTERFACE (SMIF) |
|
EN 12307:1997
|
Biotechnology - Large-scale process and production - Guidance for good practice, procedures, training and control for personnel |
|
ISO 14644-5:2004
|
Cleanrooms and associated controlled environments — Part 5: Operations |
|
BS 3636:1963
|
Methods for proving the gas tightness of vacuum or pressurized plant |
|
SEMI E62 : NOV 2006(R2012)
|
SPECIFICATION FOR 300 MM FRONT-OPENING INTERFACE MECHANICAL STANDARD (FIMS) |
|
NFC 01 371 : 85 AMD 1 1999
|
ELECTROTECHNICAL VOCABULARY - CHAPTER 371: TELECONTROL |
|
ISO 14698-1:2003
|
Cleanrooms and associated controlled environments Biocontamination control Part 1: General principles and methods |
|
ISO 14644-3:2005
|
Cleanrooms and associated controlled environments Part 3: Test methods |
|
ENV 1631 : 1996
|
CLEANROOM TECHNOLOGY - DESIGN, CONSTRUCTION AND OPERATION OF CLEANROOMS AND CLEAR AIR DEVICES |
|
ISO 13408-1:2008
|
Aseptic processing of health care products — Part 1: General requirements |
|
ISO 14644-1:2015
|
Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
|
EN 12296:1998
|
Biotechnology - Equipment - Guidance on testing procedures for cleanability |
|
ISO 14644-4:2001
|
Cleanrooms and associated controlled environments — Part 4: Design, construction and start-up |
|
SEMI E47.1 : NOV 2006
|
MECHANICAL SPECIFICATION FOR FOUPS USED TO TRANSPORT AND STORE 300 MM WAFERS |
|
ISO 10648-2:1994
|
Containment enclosures — Part 2: Classification according to leak tightness and associated checking methods |
|
EN 12469:2000
|
Biotechnology - Performance criteria for microbiological safety cabinets |
|
ISO 13408-6:2005
|
Aseptic processing of health care products Part 6: Isolator systems |
|
ISO 13408-5:2006
|
Aseptic processing of health care products Part 5: Sterilization in place |