The Research Involving Human Embryos Act 2002 requires that research on human embryos can only be conducted under a licence issued by the National Health and Medical Research Council (NHMRC) Embryo Research Licensing Committee (NHMRC Licensing Committee).

Licensable activities

Licensable activities include:

  • some uses of excess assisted reproductive technology embryos
  • the creation or use of certain other human embryos
  • research or training involving fertilisation of a human egg by a human sperm
  • other activities specified in the legislation.

Information kit

The following Information kit summarises the regulatory framework:

How to apply

Complete the relevant application form below. The instructions will help you to fill out the application. The consent checklists and additional information about obtaining proper consent will help you develop a consent process and documents that satisfy the legislative requirements.c

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. Refer to the instructions for more information. (Documents available under Downloads below).


Before anyone can be trained under a licence issued by the 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, 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.

Objective Criteria

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 section 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.

Criteria for determining 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:

The NHMRC Licensing Committee must also have regard to:

The Research Involving Human Embryos Regulations 2017 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. Refer to the Regulations to check which versions apply to your application.

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
  • 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 activity.

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 activity is given.