• EN 12128:1998

    Current The latest, up-to-date edition.

    Biotechnology - Laboratories for research, development and analysis - Containment levels of microbiology laboratories, areas of risk, localities and physical safety requirements

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    Language(s): 

    Published date:  17-03-1998

    Publisher:  Comite Europeen de Normalisation

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    Table of Contents - (Show below) - (Hide below)

    Foreword
    Introduction
    1 Scope
    2 Normative references
    3 Definitions
    4 Physical containment level classification
    5 Physical containment level 1 laboratory (PCL1)
    6 Physical containment level 2 laboratory (PCL2)
    7 Physical containment level 3 laboratory (PCL3)
    8 Physical containment level 4 laboratory (PCL4)
    Annex A (informative) Guidance on space needs and dimensions
    Annex B (informative) Method of test for the determination
            of pressure differences
    Annex C (informative) Bibliography

    Abstract - (Show below) - (Hide below)

    This European Standard specifies minimum physical requirements for biological safety for laboratories at four reference physical containment levels which are appropriate for handling microorganisms of different risk groups. This European Standard primarily addresses the containment of microorganisms which can present a risk to human health. It applies to microbiology laboratories where the handling of microorganisms in bacteriology, mycology, virology, parasitology and/or genetic modification is carried out.

    General Product Information - (Show below) - (Hide below)

    Committee CEN/TC 233
    Document Type Standard
    Publisher Comite Europeen de Normalisation
    Status Current

    Standards Referenced By This Book - (Show below) - (Hide below)

    PD 6632:1998 Biotechnology. Laboratories for research, development and analysis. Guidance on the selection of equipment needed for biotechnology laboratories according to the degree of hazard
    I.S. CR 12739:1999 BIOTECHNOLOGY - LABORATORIES FOR RESEARCH, DEVELOPMENT AND ANALYSIS - REPORT ON THE SELECTION OF EQUIPMENT NEEDED FOR BIOTECHNOLOGY LABORATORIES ACCORDING TO THE DEGREE OF HAZARD
    EN 12738:1999 Biotechnology - Laboratories for research, development and analysis - Guidance for containment of animals inoculated with microorganisms in experiments
    EN 12740:1999 Biotechnology - Laboratories for research, development and analysis - Guidance for handling, inactivating and testing of waste
    EN 13441:2001 Biotechnology - Laboratories for research, development and analysis - Guidance on containment of genetically modified plants
    EN 12741:1999 Biotechnology - Laboratories for research, development and analysis - Guidance for biotechnology laboratory operations
    S.R. CWA 15793:2011 LABORATORY BIORISK MANAGEMENT
    BS EN 12738:1999 Biotechnology. Laboratories for research, development and analysis. Guidance for containment of animals inoculated with microorganisms in experiments
    BS EN 12740:1999 Biotechnology. Laboratories for research, development and analysis. Guidance for handling, inactivating and testing of waste
    BS EN 12741:1999 Biotechnology. Laboratories for research, development and analysis. Guidance for biotechnology laboratory operations
    BS EN 13441:2002 Biotechnology. Laboratories for research, development and analysis. Guidance on containment of genetically modified plants
    CR 12739 : 1998 BIOTECHNOLOGY - LABORATORIES FOR RESEARCH, DEVELOPMENT AND ANALYSIS - REPORT ON THE SELECTION OF EQUIPMENT NEEDED FOR BIOTECHNOLOGY LABORATORIES ACCORDING TO THE DEGREE OF HAZARD

    Standards Referencing This Book - (Show below) - (Hide below)

    EN 61010-2-041:1996/corrigendum:1996 SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL, AND LABORATORY USE - PARTICULAR REQUIREMENTS FOR AUTOCLAVES USING STEAM FOR THE TREATMENT OF MEDICAL MATERIALS AND FOR LABORATORY PROCESSES
    ISO 4211:1979 Furniture — Assessment of surface resistance to cold liquids
    EN 12740:1999 Biotechnology - Laboratories for research, development and analysis - Guidance for handling, inactivating and testing of waste
    EN 1620:1996 Biotechnology - Large-scale process and production - Plant building according to the degree of hazard
    EN 12741:1999 Biotechnology - Laboratories for research, development and analysis - Guidance for biotechnology laboratory operations
    BS 3202-1:1991 Laboratory furniture and fittings Introduction
    EN 1619:1996 Biotechnology - Large-scale process and production - General requirements for management and organization for strain conservation procedures
    EN 12347:1998 Biotechnology - Performance criteria for steam sterilizers and autoclaves
    EN 61010-2-042 : 1997 SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL AND LABORATORY USE - PARTICULAR REQUIREMENTS FOR AUTOCLAVES AND STERILIZERS USING TOXIC GAS FOR THE TREATMENT OF MEDICAL MATERIALS AND FOR LABORATORY PROCESSES
    IEC 61010-2-041:1995 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-041: Particular requirements for autoclaves using steam for the treatment of medical materials, and for laboratory processes
    IEC 61010-2-043:1997 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-043: Particular requirements for dry heat sterilizers using either hot air or hot inert gas for the treatment of medical materials, and for laboratory processes
    ISO 7000:2014 Graphical symbols for use on equipment Registered symbols
    EN 12469:2000 Biotechnology - Performance criteria for microbiological safety cabinets
    EN 61010-2-043 : 1997 SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL, AND LABORATORY USE - PARTICULAR REQUIREMENTS FOR DRY HEAT STERILIZERS USING EITHER HOT AIR OR HOT INERT GAS FOR THE TREATMENT OF MEDICAL MATERIALS, AND FOR LABORATORY PROCESSES
    ISO 3864:1984 Safety colours and safety signs
    IEC 61010-2-042:1997 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-042: Particular requirements for autoclaves and sterilizers using toxic gas for the treatment of medical materials, and for laboratory processes
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