Filter results
You can narrow down the results using the filters
Resource type
Publication type
OGTR Online Services Portal Frequently Asked Questions
This document provides answers to frequently asked questions relating to the OGTR's Online Services Portal (Portal).
OGTR Online Services Portal Registration Guide
This document provides step by step instructions on how to register for the OGTR's Online Services Portal.
Classification of Notifiable Low Risk Dealings (NLRDs) - reporting form requirements
This documents helps with the correct classification of NLRDs being included in the Record of Assessment for reporting online.
OGTR Online Services Portal User Guide
This guide provides assistance from the point of logging into the OGTR Online Services Portal. It follows from the OGTR Online Services Registration Guide.
OGTR Online Services Portal NLRD Form Guide
This document provides a step by step guide on how to access the NLRD Form in the OGTR's Online Services Portal.
Guidelines for Certification of a Physical Containment Level 3 Facility - new Guidelines effective 1 December 2022
These guidelines contain the requirements for certification of a Physical Containment Level 3 (PC3) Facility issued pursuant to section 90 of the Gene Technology Act 2000 (the ACT) and state legislation.
Guidance for Certification of a Physical Containment Level 3 Facility – to be read with new Guidelines effective 1 December 2022
This guidance accompanies the Guidelines for certification of a Physical Containment Level 3 (PC3) Facility effective 1 December 2022.
Explanatory Information - Guide to Physical Containment Levels and Facility Types
This document describes the Physical Containment (PC) levels used by the Gene Technology Regulator in the certification of facilities. It also explains the categories of organisms and types of dealings intended to be contained in each facility type and PC level.
Guidance for conducting human clinical trials involving GMOs
This guidance provides basic information to organisations in Australia wishing to conduct human clinical trials involving an experimental product that is, or contains, a genetically modified organism (GMO).
Guidance on making a record of Assessment for NLRD and on responsibilities of those undertaking NLRDs
This guidance is to help Institutional Biosafety Committees (IBCs) prepare a record of Assessment (RoA).
Guidance Note - Minimum information required to submit a request to modify certifications
This guidance note indicates the minimum information that must accompany any request to modify a certification, such as a variation, suspension, lift of suspension, surrender and transfer.
Guidance for IBCs: Regulatory requirements for contained research with GMOs containing engineered gene drives
This document provides guidance for Institutional Biosafety Committees (IBCs) and researchers on the regulatory requirements for organisms containing engineered ‘gene drives’, including the physical containment (PC) level of facilities for notifiable low risk dealings (NLRDs).
Guidance on the classification of contained dealings with viral vectors
Look-up tables for classification of contained dealings with viral vectors based on the vector type, characteristics and whether in vitro or in vivo.
Guidance on making an application to vary a DNIR licence
This document provides guidance on the information required in the Application to vary a DNIR licence form for a range of common variation categories.
Guidelines for Certification of a Physical Containment Level 2 Large Scale Facility
These guidelines contain the requirements and conditions for certification of a Physical Containment Level 2 (PC2) Large Scale Facility issued pursuant to section 90 of the Gene Technology Act 2000 (the Act).
Guidelines for Certification of a Physical Containment Level 2 Large Grazing Animal Facility
The guidelines (Part A) contain the requirements for certification of a Physical Containment Level 2 (PC2) Large Grazing Animal Facility issued pursuant to section 90 of the Gene Technology Act 2000 (the Act).
Explanatory Information - Certification of Physical Containment Facilities
This document provides further details on certification, how to get a facility certified and how to maintain a certification.
Explanatory Information on the Guidelines for Accreditation of Organisations
This document provides further information about how to get accredited and how to stay accredited.
Guidelines for Certification of a Physical Containment Level 2 Plant Facility
The guidelines (Part A) contain the requirements for certification of a Physical Containment Level 2 (PC2) Plant Facility issued pursuant to section 90 of the Gene Technology Act 2000 (the Act).
Guidelines for Certification of a Physical Containment Level 2 Invertebrate Facility
The guidelines (Part A) contain the requirements for certification of a Physical Containment Level 2 (PC2) Invertebrate Facility issued pursuant to section 90 of the Gene Technology Act 2000 (the Act).
Guidelines for Certification of a Physical Containment Level 2 Laboratory
The guidelines (Part A) contain the requirements for certification of a Physical Containment Level 2 (PC2) Laboratory issued pursuant to section 90 of the Gene Technology Act 2000 (the Act).
Guidelines for Certification of a Physical Containment Level 2 Aquatic Facility
The guidelines contain the requirements for certification of a Physical Containment Level 2 (PC2) Aquatic Facility issued pursuant to section 90 of the Gene Technology Act 2000 (the Act).
Guidelines for Certification of a Physical Containment Level 2 Animal Facility
The guidelines (Part A) contain the requirements for certification of a Physical Containment Level 2 (PC2) Animal Facility issued pursuant to section 90 of the Gene Technology Act 2000 (the Act).
Guidelines for Accreditation of Organisations
The guidelines detail the requirements for, and the conditions of, accreditation.
Guidelines for Certification of a Physical Containment Level 3 Laboratory
These guidelines for certification of a Physical Containment Level 3 (PC3) Laboratory have been issued pursuant to section 90 of the Gene Technology Act 2000 (the Act) and state legislation.