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Annual Inspection Checklist for a PC3 Facility - For facilities certified or re-certified after December 2022
Checklist for annual inspection against the usual Conditions of Certification as detailed in the Gene Technology Regulator’s Guidelines for Certification of a Physical Containment Level 3 Facility.
Application Checklist for a new Physical Containment Level 3 Facility
Checklist for the inspection of a new facility against the usual Conditions of Certification as detailed in the Gene Technology Regulator’s Guidelines for Certification of a Physical Containment Level 3 Facility Version 1.0 - 1 December 2022
Application for the Certification of a Physical Containment Facility
This application is for the certification of a facility to a specified containment level in accordance with Guidelines for the Certification of Physical Containment Facilities issued under the Gene Technology Act 2000 and any applicable state legislation.
Application for a licence to conduct a human clinical trial of a GMO
This application form is for licences to conduct human clinical trials of GMOs.
Accredited Organisation Annual Report to the Gene Technology Regulator
Accredited Organisations use this form to demonstrate that they are meeting their obligations and responsibilities. Completion of the form is an condition of accreditation.
NLRD reporting import template
Use this template to record and then import NLRD details into the online reporting form.
Application for Accreditation of an Organisation
Use this form to apply for accreditation of an organisation under the Gene Technology Act 2000 and any applicable state legislation.
Notifiable Low Risk Dealing (NLRDs) Reporting Form
Use this form to notify the Regulator of any NLRDs assessed during the financial year.
Notification of change in contacts for organisation
Use this form to provide or update contact and authorised persons details for organisations and Institutional Biosafety Committees (IBCs).
Application for an inadvertent dealings licence
Complete this application if you have unintentionally obtained a GMO or did not know an organism was a GMO when you obtained it.
Application for a DIR licence for the limited and controlled release of GM plants
This application form is for dealings (activities) involving limited and controlled release of genetically modified (GM) plants into the environment.
Application for a licence for importation and processing of bulk grain
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.
Model Form – Record of Assessment for a Notifiable Low Risk Dealing (NLRD)
IBCs can use this model form when making an NLRD record of assessment (RoA) and recording that it has been given to the proponent.
Application for a licence for dealings not involving intentional release of a GMO (DNIR)
This application form must be used for applications for a licence for dealings (activities) NOT involving the intentional release of a GMO into the environment (DNIR).
Application to vary a DNIR licence
Use this form to apply for a variation of a licence for dealings not involving intentional release (DNIR) of a GMO into the environment under the Gene Technology Act 2000 (the Act).
Application to vary a DIR licence
Use this form to apply for a variation of a licence for dealings involving intentional release (DIR) of a GMO into the environment under the Gene Technology Act 2000 (the Act).
Application for a DIR licence for commercial release of GM plants
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.
Application for a confidential commercial information (CCI) declaration
Use this form to apply for a declaration that specified information is confidential commercial information (CCI) under the Gene Technology Act 2000.
Annual Inspection Checklist for a PC2 Large Scale Facility
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
Application Checklist for a Physical Containment Level 2 Large Scale Facility
Checklist against the requirements of the Gene Technology Regulator’s Guidelines for Certification of a Physical Containment Level 2 Large Scale Facility.
Application for a DIR licence involving a non-plant GMO
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.
Application for a DIR licence for commercial release of GM plants - example answers
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.
Three Monthly Checklist for a PC2 Large Grazing Animal Facility
Checklist against the conditions of certification under the Gene Technology Regulator’s Guidelines for Certification of a Physical Containment Level 2 Large Grazing Animal Facility.
Application Checklist for a Physical Containment Level 2 Large Grazing Animal Facility
Checklist against the requirements for certification under the Gene Technology Regulator’s Guidelines for Certification of a Physical Containment Level 2 Large Grazing Animal Facility.
Annual Inspection Checklist for PC2 Animal Facility
This checklist is based on the usual conditions of certification as detailed in the Gene Technology Regulator’s Guidelines for Certification of a Physical Containment Level 2 Animal Facility.