1218 results found
The NHMRC Complaints Policy sets out how NHMRC manages complaints about its activities, policies and decision-making.
Members of NHMRC’s Dietary Guidelines Governance Committee (the Governance Committee) have been appointed to consider possible conflicts of interest and potential bias across the revision of the 2013 Australian Dietary Guidelines.
NHMRC provides advice about the care of people in post-coma unresponsiveness (vegetative state) or a minimally responsive state.
Tropical medicine and healthcare services are a key pillar enabling more Australians to live and work in northern Australia, and thereby expand the north’s economic contribution to Australia.
This paper provides information on the establishment, management and governance of biobanks in Australia. A biobank is a collection of human biological material held for health and medical research. Biobanks facilitate this research, while protecting participants’ interests and privacy.
The 26th biannual report.
Rapid advances in DNA sequencing technologies now allow an individual’s whole genome to be sequenced.
Keeping research on track II was developed to provide advice on how the values and principles outlined in Ethical conduct in research with Aboriginal and Torres Strait Islander Peoples and communities: Guidelines for researchers and stakeholders can be put into practice in research.
The NHMRC and ARC Statement on Open Researcher and Contributor ID explains NHMRC's position on the ORCID researcher identifier.
The National Health and Medical Research Council (NHMRC) has established the Iodine Expert Working Group to support the review and update of the iodine Nutrient Reference Values for Australia and New Zealand (NRVs).
Ethical conduct in research with Aboriginal and Torres Strait Islander Peoples and communities: Guidelines for researchers and stakeholders provides a set of principles to ensure research is safe, respectful, responsible, high quality and of benefit to Aboriginal and Torres Strait Islander people and communities.
This resource has been developed to provide information to consumers about the human genome.
These guidelines outline ethical practice for health professionals involved in living organ and tissue donation and provides guidance on how these principles can be put into practice.