Standards

Standards I may or may not have discussed on this site that I have in my library.  This may not be a complete list.

  • ISO 1133.1 2009 – Microbiology of food and animal feeding stuffs — Guidelines on preparation and production of culture media
  • ISO 1042 1998 Laboratory glassware – one-mark volumetric flasks
  • ASNZS 2982.1 1997 – Laboratory design and construction – general requirements
  • AS 2706 2003 – Numerical Values – Rounding and Interpretation of limiting values
  • AS 1807.8 – 2000 Cleanrooms, workstations, safety cabients and pharmaceutical isolators – methods of test
  • AS 1386.1 – 1989 Cleanrooms and Clean Workstations
  • ISO 1737.1 1995 – Sterilization of health care products – Microbiological methods
  • ISO 1766521 2006 sterilization of healthcare products – moist heat guidance
  • ISO 14644.1 2002 – cleanrooms and assoc controlled environments – class of air cleanliness
  • ISO 27001.2 2013 – information technology – security techniques – ISMS requirements
  • ISO 19011 2011 – Guidelines for auditing management systems
  • ISO 17665.1 2006 – sterilization of healthcare products – moist heat
  • ISO 14698.2 2003 – Cleanroom and associated control environments – evaluation of data
  • ISO 14698.1 2003 – Cleanroom and associated control environments – biocontamintion control
  • ISO 14644.4 2001 – cleanrooms and assoc controlled environments – design const startup
  • ISO 14644.1 1999 – cleanrooms and assoc controlled environments – class of air cleanliness
  • ISO 14161 2009 – Sterilization of health care products – biological indicators
  • ISO 13408.5 2006 – aseptic processing of healthcare products -sterlisation in place
  • ISO 13408.2 2003 – aseptic processing of healthcare products -filtration
  • ISO 13408.1 1998 – aseptic processing of healthcare products – general requirements
  • ISO 11140.5 2012 Sterlisation of health care products – chemical indicators
  • ISO 11140.3 2012 Sterlisation of health care products – chemical indicators
  • ISO 11137.1 2013 Sterilization of healthcare products – Ammendment1
  • ISO 11137.1 2006 Sterilization of healthcare products -Radiation
  • ISO 11135.1 2007 Sterilization of healthcare products -Ethylene oxide
  • ISO 10993.7 2008 Biological evaluation of medical devices-Ethylene oxide sterilization residuals
  • ISO 10993.7 2008 Biological evaluation of medical devices-Ethylene oxide sterilization residuals – TECHNICAL CORRIGENDUM 1
  • ISO 10993.1 2009 Biological evaluation of medical devices
  • ISO 9001 (2015) – Quality management systems
  • ISO 9001 (2015) -what does it mean in the supply chain
  • ISO 9001 (2015) -how to use it
  • ISO 9001 (2008) – Quality management systems
  • ISO 9001 (2008) – the dumb ass aerospace version
  • ISO 19011 (2011) – Guidelines for auditing management systems
  • ISO 8871.5 2003 – Elastomeric parts for parenterals and for devices for pharmaceutical use – Functional requirements and testing
  • ISO 8871.4 2003 – Elastomeric parts for parenterals and for devices for pharmaceutical use – Biological requirements and test methods
  • ISO 8871.3 2003 – Elastomeric parts for parenterals and for devices for pharmaceutical use – Determination of released-particle count
  • ISO 8871.2 2003 – Elastomeric parts for parenterals and for devices for pharmaceutical use – identification and characterization
  • ISO 8871.1 2003 – Elastomeric parts for parenterals and for devices for pharmaceutical use
  • ISO 8573.3 1999 – Compressed Air Test Methods for Humdity
  • ISO 8573.7 2003 Compressed Air
  • ISO 8573.1 2010 Compressed Air
  • ISO 8573.1 2010 Compressed Air – technical corrigendum
  • ISO 4787 2010 – Laboratory Glassware – Volumetric Instruments – Methods for testing of capacity and for use