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Guidelines for the certification of physical containment facilities
These guidelines describe the requirements for the certification of each level and type of physical containment facility as per section 90 of the Gene Technology Act 2000 (the Act).
Inspection checklists for physical containment facilities
These checklists set out the criteria for an inspection against the usual conditions of certification of physical containment facilities.
Application checklists for the certification of physical containment facilities
These checklists list the requirements of the Gene Technology Regulator’s guidelines for certification of a physical containment facility.
Guidelines and checklists for certification of PC3 facilities
Documents supporting applications for the certification of Physical Containment Level 3 (PC3) facilities.
Annual reports on the Operations of the Gene Technology Regulator
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.
Quarterly activities reports
These reports detail the monitoring and compliance activities by the Office of the Gene Technology Regulator (OGTR) for each quarter.
Application and reporting forms
Forms for licence applications, organisation accreditation, and reporting obligations.
Biology documents
These documents are prepared to inform the Gene Technology Regulator's Risk assessment and Risk Management Plans in response to licence applications for clinical trials, field trials or release of genetically modified organisms into the environment.
Community attitudes to gene technology reports
These surveys help gauge the state of public awareness, identify knowledge gaps and track changes in awareness and attitudes over time.
Information for Institutional Biosafety Committees
Useful resources for IBCs covering records of assessment, classification of NLRDs and contained dealings.
Monitoring and compliance protocols
The OGTR has developed a range of documents to provide organisations and interested parties with guidance on monitoring and compliance activities under the Gene Technology Act 2000.
Risk assessment reference documents
These documents support the Risk Assessment and Risk Management Plans (RARMPs) prepared for applications for dealings involving intentional release (DIRs) of GMOs into the environment. They address matters common to many DIR risk assessments and are referred to in relevant RARMPs.
Guidelines and checklists for certification of PC2 facilities
Documents supporting applications for the certification of Physical Containment Level 2 (PC2) facilities.
Guidelines and checklists for certification of PC1 facilities
Documents supporting applications for the certification of Physical Containment Level 1 (PC1) facilities.