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The Gene Technology Act 2000 requires Gene Technology Regulator to report annually on their operations. The reports are produced for the Minister as soon as practicable after the end of each financial year.
The report describes the roles and responsibilities of the Gene Technology Regulator (the Regulator) and the Office of the Gene Technology Regulator (OGTR) during 2022-23.
Use this form to apply for a declaration that specified information is confidential commercial information (CCI) under the Gene Technology Act 2000.
This document provides examples of the details you may need to supply in describing the information for which you are seeking declaration as CCI.
Application for declaration that specified information is CCI - information for completing the CCI form
This document contains general information about the CCI application form and specific information for individual sections and questions in the form.
This fact sheet aims to clarify what level of notification and advance warning is required for low-level (PC1 and PC2, excluding PC2 Large Scale) certified facilities that undergo maintenance work.
This decision tree provides assistance on which type of form needs to be completed when conducting maintenance or repair work on a low level containment facility.
This Statement of Intent outlines the activities of the Gene Technology Regulator (the Regulator) and the Office of the Gene Technology Regulator (OGTR) over the next 3 years from 2023-2026.
This documents helps with the correct classification of NLRDs being included in the Record of Assessment for reporting online.
Accredited Organisations use this form to demonstrate that they are meeting their obligations and responsibilities. Completion of the form is an condition of accreditation.
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 limited and controlled release.
This application form is for dealings (activities) involving limited and controlled release of genetically modified (GM) plants into the environment.
This infographic gives a brief description of the difference between OGTR and FSANZ regulatory remits, where the OGTR conducts risk analysis and licensing for commercial cultivation, while FSANZ conducts food safety assessments, approves food for sale and sets labelling requirements.