This page contains information relating to applying for licences to use excess assisted reproductive technology (ART) embryos, create or use certain other embryos, conduct certain research or training involving fertilisation of a human egg by a human sperm, or fertilisation of an animal egg with a human sperm for the purpose of testing sperm quality.
How to apply
Please complete the application form below. The instructions and the Information Kit will help you to fill out the application.
Please also refer to the Prohibition of Human Cloning for Reproduction Act 2002 (PHCR Act) and the Research Involving Human Embryos Act 2002 (RIHE Act).
Embryo Biopsy Training Licence Applications
If you are applying for a licence to conduct training in embryo biopsy using excess ART embryos, you can fill out the shorter application form below. Please refer to the instructions for more information.
Before anyone can be trained under a licence issued by the NHMRC Embryo Research Licensing Committee (NHMRC Licensing Committee), the person must be authorised to use embryos under the licence. If prospective trainees have been identified before the licence is issued, please include their names and details in the application form.
Additional trainees can also be added after the licence has been issued by applying for a variation to the licence. The information specified at item 2.8 of the application form must be included in the variation application for each additional trainee.
The Objective Criteria describe the developmental characteristics of embryos which can be determined to be unsuitable for implantation (see paragraph (b) of the definition in s.7 of the RIHE Act). If a research project requires the use of fresh embryos the Objective Criteria must be used to determine which embryos can be donated to the licensed research.
What criteria are used to determine whether a licence should be issued?
The RIHE Act sets out criteria that the NHMRC Licensing Committee must consider before it issues a licence authorising the use of excess ART embryos or the creation and/or use of other embryos.
According to these criteria, the NHMRC Licensing Committee must be satisfied that:
- appropriate protocols are in place to enable proper consent to be obtained before an excess ART embryo or human egg is used or other embryos are created or used and to ensure adherence to any restrictions specified by the persons for who gave consent to the use; and
- the proposed project has been considered and approved by a Human Research Ethics Committee that is constituted in accordance with, and acting in compliance with, the NHMRC's National Statement on Ethical Conduct in Human Research 2007.
The NHMRC Licensing Committee must also have regard to:
- restricting the number of excess ART embryos, other embryos or human eggs to that likely to be necessary to achieve the goals of the research or activity proposed in the application;
- the likelihood of significant advance in knowledge or improvement in technologies for treatment as a result of the use of excess ART embryos or human eggs or the creation or use of other embryos, proposed in the application, which could not reasonably be achieved by other means;
- any relevant guidelines, or parts of guidelines, issued by the NHMRC, as prescribed in the Regulations. Currently the relevant Guidelines are the National Statement on Ethical Conduct in Human Research (2007) and the Ethical Guidelines on the use of Assisted Reproductive Technology in Clinical Practice and Research (2007); and
- the Human Research Ethics Committee's assessment of the application.
The Research Involving Human Embryos Regulations 2003 specify which versions of the National Statement and the Ethical Guidelines are prescribed at any given time. This may not always be the latest version of the guideline. Please refer to the Regulations to check which versions apply to your application.
What is proper consent for the use of excess ART embryos and human eggs and the creation and/or use of other embryos?
The legislation makes it illegal to use an excess ART embryo or human egg or to create or use an embryo for licensed research without consent having been provided, in writing, by all responsible persons.
The legislation defines the people responsible for an embryo as:
- the gamete providers and their partners, if any, at the time the gametes were donated;
- the woman for whom the embryo was created for the purpose of achieving her pregnancy; and
- her partner if different from the gamete provider.
The legislation defines the person responsible for a human egg as the woman who was the biological donor of the egg.
In relation to embryos created under a licence, each person whose reproductive material, genetic material or cell was donated for use under the licence is a responsible person who must give consent.
Before consenting, all responsible persons must have been provided with written information describing the proposed research.
Before issuing a licence, the NHMRC Licensing Committee must be satisfied that the consent protocols are appropriate and that the donors will receive appropriate information to enable them to make an informed decision about whether to donate the embryo, egg, genetic material or cell to research.
Guidelines also require that counselling is offered and an explanation about the proposed research is given.