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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.
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 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.
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.
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).
These checklists list the requirements of the Gene Technology Regulator’s guidelines for certification of a physical containment facility.