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The Report of the Independent Review of the Prohibition of Human Cloning for Reproduction Act 2002 and the research involving human embryos Act 2002 offers a review of legislation regarding the use of human clones for reproduction and the use of human embryos in research.
Genetic tests are easily purchased by consumers, often over the internet and usually without the involvement of a medical professional. These tests can be used in diagnosing medical conditions or pre-dispositions. The statement highlights issues for medical professionals and consumers regarding the use of health-related genetic testing.
The use of mitochondrial donation in Australia is regulated by a licensing scheme.
The Discussion Paper: Options to reach gender equity in the Investigator Grant scheme presents 4 options to offset the systemic disadvantage faced by women in health and medical research, as reflected in the attrition of female applicants with seniority in the Investigator Grant scheme.
The Vitamin K administration to newborn infants to prevent vitamin K deficiency bleeding in infancy recommendations for Vitamin K to be given to newborn children.
Engaging Aboriginal and Torres Strait Islander people in guideline development Engagement is a relationship built on trust and integrity
10 of the Best research projects 2013 showcases 10 Australian health and medical research projects chosen from among the thousands of NHMRC-funded medical research projects underway in Australia. These projects illustrate the extraordinary quality and diversity of work being undertaken with NHMRC support.
10 of the Best Research Projects 2009 showcases 10 Australian health and medical research projects chosen from among the thousands of NHMRC-funded medical research projects in Australia.
This page includes information on guidelines and tools about: Assisted Reproductive Technology clinical ethics decision-making for pandemics research involving Aboriginal and Torres Strait Islander peoples health privacy organ and tissue donation and transplantation payment of participants in research peer review and ethical review embryo research, stem cells and human cloning quality assurance and evaluation activities participant information and consent forms.
To improve clinical trial start-up times, we developed the Good Practice Process for Site Assessment and Authorisation Phases of Clinical Trial Research Governance (the Good Practice Process).
If you have received an MRFF grant and circumstances have changed – for example, there has been a delay in your research activity – you can apply to vary your grant.
Outcomes of Synergy Grants funding rounds.
Licence holders are responsible for ensuring that their organisations comply with licence conditions. Each person who is identified in the licence conditions as an authorised person must be fully informed about the licence and its conditions and the requirements of the legislation and any corresponding state or territory law.