We have published a wealth of information on Australian health and medical research, and on specific issues relating to Australian health and health care. These include statements, strategies, guidelines and other reports – all of which are publicly available.
Read our latest publications
This guide supports the implementation of the Australian code for the care and use of animals for scientific purposes 8th edition (2013) by providing advise about the specific and unique needs of Australian native mammals can be met when these animals are used for scientific purposes.
It provides information for investigators, institutions, animal ethics committees and all those involved in the care and use of Australian native mammals for scientific purposes.
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 number of direct to consumer DNA tests consumers can buy over the internet, without the involvement of a doctor, has been rising.
This resource is to inform consumers about test accuracy, privacy legislation and what it may mean for personal insurances and blood relations.
This information has been developed for health practitioners to support discussion with men and their families about prostate-specific antigen testing for prostate cancer. It covers benefits, possible risks, current research and frequently asked questions.
The Guidelines approved under Section 95A of the Privacy Act 1988 are issued for the purposes of Australian Privacy Principles (APPs) and sections 16B(2) and 16B(3) of the Privacy Act.
The Privacy Legislation Amendment Act 2006 (Cth) made changes to the Privacy Act 1988(Cth) (the Privacy Act) to allow health practitioners to disclose patient’s genetic information, whether or not they give consent, in circumstances where there is reasonable belief that doing so is necessary to lessen or prevent a serious threat to the life, health or safety of their genetics relative(s). The amendments do not oblige disclosure of information but provide the framework for this to occur under the appropriate circumstances.
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.
See more 10 of the Best
Discrimination against an individual can appear in many forms. As DNA testing increasingly identifies differences in the genetic make-up of individuals, it becomes possible that people will be discriminated against based on genetic information.
Using information about genetic predisposition to disease is a key part of personalised medicine. This resource has been developed to provide information to consumers about personalised medicine and genetics.
DNA testing can be used for a number of purposes not related to health. One area of interest is the potential for DNA testing and genetic profiles in sport applications such as talent identification, individualised training programs and avoidance of sport-related injury.
This resource has been developed to provide information to consumers about the human genome.
The Clinical Practice Guidelines for the management of overweight and obesity in adults, adolescents and children in Australia is intended for use by clinicians including general practitioners.
This document includes NHMRC priorities, the major health issues identified for the 2013-15 period, how NHMRC will deal with those issues and a strategy for medical research and public health research.
The purpose of the Australian code for the care and use of animals for scientific purposes (the Code) is to promote the ethical, humane and responsible care and use of animals used for scientific purposes. It provides guidance for investigators, institutions, animals ethics committees, animal carers and all those involved in the care and use of animals for scientific purposes. Further information about the background and purpose of the Code is also available.
A web version of the Code is provided below.
A PDF version of the Code is available under 'Downloads'
Guidance documents about implementation of Section 7: Cosmetic Testing of the Code are available under ‘Downloads’.
This Staying healthy: Preventing infectious diseases in early childhood education and care services replaces the 4th edition and represents an increased focus on a risk-management approach to infection prevention and control principles in daily care activities.
Rapid advances in DNA sequencing technologies now allow an individual’s whole genome to be sequenced.
This Clinical Practice Guideline for the management of Borderline Personality Disorder will assist health professionals to diagnose, treat and manage BPD in adolescents and adults.
To ensure we can make healthy food choices, we need dietary advice based on the best scientific evidence. This Guideline seeks to offer the best advice on dietary patterns that promote optimal health and wellbeing for the generally healthy Australian population.
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.
This factsheet aims to support people to: understand the basics of DNA, genes and chromosomes; consider whether to get tested; understand the potential outcomes of the genetic testing process; and find more information and support.
The full title of this factsheet is: DNA Genetic Testing in the Australian Context: A Statement from the National Health and Medical Research Council.
This handbook outlines the requirements and procedures for the certification of institutions under our National Certification Scheme of Institutional Processes Related to the Ethical Review of Multi-centre Research.
The handbook is currently under review. Before commencing steps to apply for certification, please contact us at HREC.email@example.com for further advice.
The Infant Feeding Guidelines are written to assist health workers provide consistent advice about breastfeeding and infant feeding. They provide a review of the evidence, and clear evidence-based recommendations on infant feeding for health workers.
The aim of the statement is to provide the general public with information on the assessment and management of cancer clusters. It is intended to support guidelines issues by State and Territory Departments and Cancer Councils.
The Australian Drinking Water Guidelines (the Guidelines) provide guidance to water regulators and suppliers on monitoring and managing drinking water quality.
April 2023: Please note NHMRC has identified an error of minor significance in the September 2022 update to the microbial water quality guidance (Chapter 5 and Appendix 3 of the Guidelines). Information about the error and the proposed corrections that will be made to the next version of the Guidelines are outlined below in the Public Notice.
The Procedures and requirements for meeting the 2011 NHMRC standard for clinical practice guidelines are designed to support guideline developers, including those seeking NHMRC approval, to ensure that guidelines are developed to the highest standard.
The Community water planner: A tool for small communities to develop drinking water management plans was a web-based tool developed to help assess and manage the risks in remote Australian community water supplies. This tool is no longer available.
Iodine is an essential nutrient that humans need in very small quantities. The thyroid uses iodine to produce hormones vital to ensure normal development of the brain and nervous system before birth, in babies and young children. For this reason, it is very important that pregnant and breastfeeding women get enough iodine.
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.
Road map II: A strategic framework for improving the health of Aboriginal and Torres Strait Islander people through research
Road map II: A strategic framework for improving the health of Aboriginal and Torres Strait Islander people through research will be used by the NHMRC’s Research Committee to identify research topics requiring priority funding.
The paper identifies key issues that should be considered in relation to genetic testing, and identifies relevant resources, guidelines, standards, and requirements that are pertinent for the delivery of genetic testing in Australia.
Human Ethics Committees have a difficult and sometimes controversial role in guiding the Australian research community’s work with people. Challenging ethical issues in contemporary research on human beings focuses on some of the most challenging ethical issues using case studies and through discussions.
The Guidelines to promote the wellbeing of animals used for scientific purposes: The assessment and alleviation of pain and distress in research animals (2008) provide guidance on how to support and safeguard the wellbeing of animals used for scientific purposes.
Notice: This publication is more than five years old and may no longer reflect current evidence or best practice.
The Australian Guidelines for Water Recycling: Augmentation of drinking water supplies builds on guidance provided in Phase 1 on the planned use of recycled water (treated sewage and stormwater) to top up drinking water supplies.
NHMRC provides advice about the care of people in post-coma unresponsiveness (vegetative state) or a minimally responsive state.
These guidelines aim to protect Australians from threats posed by the recreational use of coastal, estuarine and fresh water environments. These guidelines are currently being updated by NHMRC’s Recreational Water Quality Advisory Committee.
This criteria must be used for determining embryos that are considered unsuitable for implantation and that may be used for research. The NHMRC will continue to work with the scientific community to update and refine these Objective Criteria as additional scientifically authenticated information becomes available.
These guidelines outline ethical principles for health professionals involved in donation after death and provide guidance on how these principles can be put into practice.
This booklet aims to help people think through some ethical issues and make decisions about living organ and tissue donation. If you are thinking of making a living donation, the doctors caring for you can give you more information that is relevant to your situation.
The booklet aims to help people think through some ethical issues and make informed decisions about organ and tissue donation after death.
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.
The Australian Code for the Responsible Conduct of Research, 2007 (the 2007 Code) guides institutions and researchers in responsible research practices and promotes research integrity. It assists institutions in developing their own employee codes of conduct and procedures for the investigation of allegations of research misconduct by providing a comprehensive framework of acceptable academic standards.
This document outlines required essential nutrient intake believed adequate to meet the nutritional needs of the majority of healthy people to prevent deficiency. The document can be used by health professionals to assess the likelihood of inadequate intake in individuals or groups.
Cultural Competency in health: A guide for policy, partnerships and participation is designed to help policy makers and stakeholders develop culturally competent policies throughout the health system.
Keeping research on track: a guide for Aboriginal and Torres Strait Islander peoples about health research ethics was designed for Aboriginal and Torres Strait Islander communities when they are considering conducting or being involved with health research.