ISO : International Organization for Standardization in Pharmaceuticals : Pharmaguideline
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  • Feb 1, 2011

    ISO : International Organization for Standardization in Pharmaceuticals

    ISO guidelines for Cleanrooms and associated controlled environments and Bio-contamination Control for Pharmaceuticals.
    ISO has covered 18000 standards that are applicable to almost all type of industries but only some of them are used in pharmaceuticals as guidelines for area qualification

    Following are the ISO Standards followed by the pharmaceutical industries for non-viable particles in the classified area.
    ISO 14644 Standards Cleanrooms and associated controlled environments
    ISO 14644-1:1999 Classification of Air Cleanliness
    ISO 14644-2:2000 Testing and Monitoring to prove Compliance
    ISO 14644-3:2005 Metrology & Test Methods
    ISO 14644-4:2001 Design, Construction and Start-up
    ISO 14644-5:2004 Operations

    ISO 14644-6:2007 Vocabulary
    ISO 14644-7:2004 Separative Devices
    ISO 14644-8:2006 Classification of Airborne Molecular Contamination
    ISO 14644-9 Clean Surfaces
    ISO guidelines for viable count in classified area i.e. clean room area.
    ISO 14698 Standards
    ISO-14698-1 Bio-contamination Control — General Principles
    ISO-14698-2 Evaluation & Interpretation of Bio-contamination Data
    ISO-14698-3

    Also Read:
    Complete List of ISO standards
    HVAC System Validation Tests
    What is HEPA filter?
    HVAC Design for Pharmaceutical Facilities
    HVAC Validation

    2 comments: Post Yours! Read Comment Policy ▼

    1. Is ISO 9001 is applied by pharmaceuticals now? When I was working back in 2004, there was ISO 9001:2000 ;Quality management system

      ReplyDelete
    2. Hi, i am getting ready for ISO 9001:2015 Up gradation, can anyone tell me what should be next issue no. for Manual, as this applicable to new revised standard.either 00 or 01.?

      ReplyDelete

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