Containment requirements that must be met in order for a Physical Containment level 2 (PC2) animal facility to be certified by the gene technology regulator (the Regulator).

Section 90 of the Gene Technology Act 2000

These are the requirements for the certification of a PC2 Animal Facility issued under section 90 of the Gene Technology Act 2000 (the Act) and, as applicable, corresponding State legislation. These requirements apply to applications for certification of PC2 Animal Facilities received on or after the day on which these guidelines take effect.

To be granted certification, a facility must meet each of the requirements for certification of a PC2 Animal Facility, unless the facility receives a written exemption from meeting a particular requirement from the Regulator or a delegate of the Regulator. Additional conditions may also be imposed on the facility by the Regulator or delegate of the Regulator.

Definitions and acronyms

aerosolSuspension in air of finely dispersed solids and/or liquids.
anteroomAn area or room between a pair of doors through which access is gained to the work area inside a facility.

The anteroom must not be used for performing any dealings other than transport of GMOs.
autoclavePressure steam steriliser.
dealing or deal withIn relation to a GMO, means the following:
  1. conduct experiments with the GMO;
  2. make, develop, produce or manufacture the GMO;
  3. breed the GMO;
  4. propagate the GMO;
  5. use the GMO in the course of manufacture of a thing that is not the GMO;
  6. grow, raise or culture the GMO;
  7. import the GMO;
  8. transport the GMO;
  9. dispose of the GMO;
and includes the possession, supply or use of the GMO for the purposes of, or in the course of, a dealing mentioned in any of the paragraphs (a) to (i).
decontamination A physical or chemical process which removes, kills or renders non-viable the GMOs used. In the case of micro-organisms this may not necessarily result in sterility.
  1. ecosystems and their constituent parts;
  2. natural and physical resources; and
  3. the qualities and characteristics of locations, places and areas.
facilityThe whole of the space that is to be certified by the Regulator to a specific level of containment.
GMGenetically modified.
GMOGenetically modified organism.
micro-organismAn organism too small to be viewed by the unaided eye, including bacteria, fungi, viruses and some multicellular organisms. For the purposes of these guidelines, this definition includes replication defective viral vectors.
OGTROffice of the Gene Technology Regulator.
PC2Physical Containment Level 2.
personal protective equipmentAny devices or equipment, including clothing, designed to be worn or held by a person on its own, or part of a system, to protect against exposure to GMOs.
pestAn unwanted organism that could cause cross-contamination within the facility or compromise containment of the GMO.
primary containerThe container directly surrounding the GMO.
risk group 2 organismAn organism that satisfies the criteria in AS/NZS 2243.3 for classification as Risk Group 2
sealedAble to contain all GMOs or the reproductive material of GM plants or GM aquatic organisms (including pollen or gametes) being transported or stored, and able to remain closed during all reasonably expected conditions of transport and storage.
secondary containerThe container immediately surrounding the primary container.
the RegulatorThe Gene Technology Regulator.
viableMicro-organisms, cells and cell cultures:
  • able to survive or multiply even though resuscitation procedures may be required, e.g. when sub-lethally damaged by being frozen, dried, heated, or affected by chemicals, including decontamination agents.
Other organisms, whole or part:
  • able to live and grow independently of its parent or source organism, or able to reproduce or contribute genetic material to reproduction (e.g. sperm, ova, pollen, seeds, vegetative propagules).
work areaAny area inside a facility that is not performing the function of an anteroom.
Dealings with GMOs other than transport, storage and disposal may only take place in the work area and any dealings with GMOs in the work area are subject to the conditions on the certification instrument.

Unless defined otherwise in this document, words and phrases used in this document have the same meaning as in the Act and the Gene Technology Regulations 2001 (the Regulations).

Words in the singular include the plural and words in the plural include the singular.

Where any word or phrase is given a defined meaning, any other part of speech or other grammatical form in respect of that word has a corresponding meaning.

Facility and fittings requirements

1. The facility to be certified must be a fully enclosable space bounded by walls, doors, windows, floors and ceilings. The facility doors and windows must be lockable or otherwise able to be secured.
    NOTE: The walls, doors, windows, floors and ceilings form the physical containment barrier of the facility where dealings with GMOs will be conducted.

    This barrier protects all spaces outside the facility, including internal spaces of buildings in which a certified facility is located, and the environment.
2. The facility must have an anteroom.
    NOTE: If no dedicated anteroom is present, then an adjacent room, either uncertified or certified may act as an anteroom subject to approval by the Regulator. The Regulator may attach conditions to the room
    acting as the anteroom to the Animal Facility.
3. The facility boundaries (walls, doors, floors, ceilings etc.) must be designed to prevent the escape of the animals being contained.

4. If the facility has drainage exits, including hand basins, they must be fitted with barriers (e.g. screens, water traps). This barrier must be of a suitable size so to prevent the movement either in or out of the facility of animals via the drains.
    NOTE: Hand basins can utilise a water trap. If GM micro-organisms are present, then the barriers must be of a suitable type and size to prevent the movement of invertebrates across the facility boundary.
5. Any openings in the walls, ceiling or roof must be filtered or screened at the facility boundary to prevent the entry or exit of animals, including invertebrates. The filter or screen must be of a material mechanically strong enough to withstand any airflow load, remain undamaged with regular cleaning, and resist corrosion and penetration by animals.
    NOTE: If GMOs with the potential to be disseminated are present, then the filters or screens must be of a suitable type and size to prevent the movement of invertebrates across the facility boundary.
6. Open spaces between and under benches, cabinets and equipment in the facility must be accessible for decontamination.
    NOTE: The requirement for access to open spaces is to allow for easier decontamination of spills and to prevent any persistence of GMOs on the floor.

Dealings involving GM micro-organisms

If any of the dealings proposed to be conducted in the facility will involve GM micro-organisms, the facility must meet the following requirements in addition to all other requirements listed:

7. The following surfaces in the facility must be smooth, impermeable to water, easily cleanable, and resistant to damage by the cleaning agents and/or decontamination agents that will be used in the facility:
  1. walls, floors, doors, windows and benches;
  2. furniture, including seating; and
  3. any other surfaces, where contamination is likely to occur or where decontamination is required.
8. The facility must contain either a dedicated wash-basin fitted with taps of the hands-free operation type or some other means of decontaminating hands.
    NOTE: Decontamination of hands is considered an important means of preventing unintentional release of GM micro-organisms and protecting the health of facility personnel. If wash-basins are to be used, the provision of hand-operated taps is not acceptable, as they can be a source of contamination.

    Alternatives to wash-basins, such as dispensers filled with decontaminant solutions, are considered suitable.
9. If any proposed dealings in the facility are with GMOs that are Risk Group 2 organisms, then eyewash equipment (either plumbed eyewash equipment or single-use packs of sterile eye irrigation fluids) must be provided within the facility.
    NOTE: The Regulator does not require the placement of more than one piece of eyewash equipment in the facility.

    Consideration should be given to the wearing of appropriate forms of eye protection.
10. If any proposed dealings in the facility with GM micro-organisms will produce aerosols containing Risk Group 2 GM micro-organisms, then the facility must contain a biological safety cabinet or other equipment specifically approved in writing by the Regulator that is designed to contain aerosols.
    Where a Class I or Class II biological safety cabinet is installed, it must be installed in accordance with the requirements of AS 2252.4.
11. Where the facility complies with AS/NZS 2243.3, in relation to backflow prevention requirements for water supplied to the facility, no backflow prevention assessment is required.

12. Where the facility does not comply with AS/NZS 2243.3, an assessment must be undertaken to determine whether backflow prevention on the water supplied to the facility is necessary.
    NOTE: Consideration should be given in the assessment to the potential hazards of the GMOs that are proposed to be dealt with in the facility; the presence of cross-connections, devices or systems that may cause contamination of a water supply connected directly or indirectly to any part of a water service; and the likelihood of a backflow event.

    If it is determined that backflow prevention is necessary then backflow prevention measures, appropriate for the risks posed by the GMOs proposed to be dealt with in the facility, must be implemented.

    Documentation which demonstrates the backflow prevention assessment, and any backflow prevention measures implemented, must be kept and made available to the Regulator if requested.

      NOTE: AS/NZS 3500.1 specifies the requirements and methods for the prevention of contamination of potable water within the water service and the water main, and provides for the selection and installation of backflow
      prevention devices.
13. Designated storage or hanging provisions for personal protective equipment must be available in the facility.

Capacity to comply with certification conditions

14. The applicant must be able to demonstrate a capacity to comply with the conditions of certification that will generally be applied to a certified PC2 Animal Facility. These conditions are found in Part B of this document.

Information required with application forms

15. In addition to identifying the rooms to be certified, the floor plans for the facility submitted with the application must clearly identify rooms or spaces that are lifts, toilets, bathrooms, kitchens, lunch rooms and offices with carpets.
    NOTE: The Regulator would not usually certify the above rooms or spaces as part of the certified facility.