Research and Ethics Office
Ethical conduct of research activities involving human participants is governed by guidelines contained in legislation and policies. The primary purpose of these guidelines for the conduct of research activities involving human participants is to ensure the protection of the welfare and the rights of human participants.
The secondary purpose is to facilitate research that is, or will be, of benefit to the researcher's community or humankind. Barwon Health has established the Human Research Ethics Committee to administer these guidelines, to provide assistance to researchers in the consideration of ethical issues involved in research and to apply policy.
The Research and Ethics Office is involved in a number of activities including:
- Providing information, support and guidance to researchers regarding research ethics
- Providing the secretariat for Human Research Ethics Committee and the Research Review Committee
- Providing administrative support for the Human Research Ethics Committee
- Liaising between the Committees and applicants
- Conducting a preliminary review of applications and providing feedback to applicants prior to submission of the application for ethics approval
- Contributing to monitoring of all approved research projects
- Developing, implementing, reviewing and updating policies and procedures relating to research ethics
- Ensuring that the Committees and Barwon Health are compliant with relevant State and Federal legislation relating to the ethical conduct of research
- Reporting to Barwon Health, the National Health and Medical Research Council, and other relevant organisations.
This Committee reviews for
- Barwon Health
- Colac
- SJOG Geelong
- Geelong Private Hospital
- South West Health Care (Warrnambool)
- Jointly with Deakin University
Applications from other sites are considered on an individual basis.
Useful links
National Statement on Ethical Conduct in Human Research (2007
Australian Code for the Responsible Conduct of Research
DHS Common Application Forms
NEAF
VMIA Clinical Trials
Good Clinical Practice
Qualitative Research Methods
Research Quality Framework
Requirements of the Health (Radiation Safety) Regulations 1994
Code of Practice for the Exposure of Humans to Ionising Radiation for Research Purposes (2005)
Guardianship and Administration Act 1986 (Amended)
Privacy principles compared
Clinical trial randomisation tool
Clinical trial tools
Uniform Requirements for Manuscripts Submitted to Biomedical Journals
New Zealand Clinical Trials and Research Providers Directory
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