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This application form is for dealings (activities) involving limited and controlled release of genetically modified (GM) plants into the environment.

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This is a hypothetical case study provided as an example. It should not be cited as evidence in an application. Although the data and discussions are representative, this example may not include all  considerations needed when assessing risks from a proposed GM plant commercial release.

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This application form is for dealings (activities) involving the release of GM plants into the environment that would not qualify as a limited and controlled release.

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Use this form for applications for a licence for dealings (activities) with a non-plant GMO involving intentional release (DIR) of the GMO into the environment under the Gene Technology Act 2000.

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Use this form to apply for a licence for importation and processing (devitalisation) of bulk grain containing GMOs that are authorised for cultivation or food or feed use in the country of origin.

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This checklist is based on the requirements for certification under the Gene Technology Regulator’s Guidelines for Certification of Physical Containment Facilities PC1 Facility.

Home > Ongoing regulatory compliance

You can request changes to a facility certification such as a variation, suspension, lift of suspension, surrender, and transfer. Find out how the process works and how to lodge an application.

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Checklist for annual inspection against the usual Conditions of Certification of the Gene Technology Regulator’s Guidelines for Certification of a Physical Containment Level 2 Large Scale Facility

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This checklist is based the usual conditions of certification as detailed in the Gene Technology Regulator's Guidelines for Certification of a Physical Containment Level 2 Constant Temperature Room.

Home > Resources > Publications

Checklist against the requirements of the Gene Technology Regulator’s Guidelines for Certification of a Physical Containment Level 2 Large Scale Facility.