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Our Open Access Policy (the Policy) is underpinned by the principle that publicly-funded research should be shared openly and at the earliest possible opportunity. Open access is about making research outputs freely available to use and share, which is distinct from simply 'free to read'.
On 15 November 2022, the National Health and Medical Research Council (NHMRC) co-hosted an online workshop with the CHF to commence the review of the Statement on Consumer and Community Involvement in Health and Medical Research (2016) (the Statement). See also consumer and community engagement
Tools to assess risk of bias Ongoing research is helping to make it easier for developers to find good practice tools for assessing risk of bias.
This document provides advice on the conduct of animal-based studies to ensure that the studies are rigorous, transparent and reproducible and lead to useful outcomes. It is in line with the Australian Code for the care and use of animals for scientific purposes, 8th edition (2013), which is adopted into legislation across Australia.
Consultation on options to reach gender equity in the Investigator Grant scheme: Consultation closed
NHMRC's vision is a gender diverse and inclusive health and medical research workforce to take advantage of the full range of talent needed to build a healthy Australia. NHMRC has completed its consultation on options to reach gender equity in the NHMRC Investigator Grant scheme.
Rapid advances in DNA sequencing technologies now allow an individual’s whole genome to be sequenced.
This report advises the NHMRC Chief Executive Officer on the current needs for research and clinical guidance for ME/CFS in Australia.
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.
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.
NHMRC’s Research Impact Track Record Assessment (RITRA) framework requires researchers to report on past research impacts in their applications for Investigator and Synergy Grants and requires peer reviewers to assess and score these reported impacts. Implementation of this framework is intended to provide an incentive for researchers to consider future impact when planning and conducting research, ideally leading to an increase in the translation of NHMRC-funded research and improved public health. The RITRA framework evaluation report describes the results of a process evaluation that sought to determine whether the RITRA framework has been implemented as intended.
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.
Members of the Council of National Health and Medical Research Council (NHMRC), 1 July 2021 to 30 June 2024.
This guide supports the implementation of the Australian code for the care and use of animals for scientific purposes 8th edition (2013) by providing advice about how 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.Notice: This publication is more than 5 years old and may no longer reflect current evidence or best practice.