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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.
This document provided guidance to researchers and Human Research Ethics Committees on the complex considerations necessary in the conception, design and conduct of appropriate research in Aboriginal and Torres Strait Islander communities.
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.
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.
This manual demonstrates the need for clinical ethics capacity in Australian health care organisations and provides guidance for institutions wishing to establish or strengthen an existing clinical ethics service.
The full title of this factsheet is: DNA Genetic Testing in the Australian Context: A Statement from the National Health and Medical Research Council.
The Australian Health Ethics Committee is concerned with the ethical implications of medical research and practice and of health care in general. One of the committee's major current interests is in the ethics of health care resource allocation. This is the second paper of a series on this topic.
NHMRC provides advice about the care of people in post-coma unresponsiveness (vegetative state) or a minimally responsive state.