Human ethics

Conducting research about people and their data

Any research conducted with or about people, their data, or their tissue is considered Human research, according to the National Statement on Ethical Conduct in Human Research 2025 (the National Statement), and requires ethical approval prior to commencing research. Human participation includes the involvement of human participants in the following activities:

  • surveys, interviews or focus groups;
  • psychological, physiological or medical testing or treatments;
  • having their personal documents or other materials accessed;
  • observation by researchers;
  • collection and use of their body organs, tissues or fluids (e.g. skin, blood, urine, saliva, hair, bones, tumour and other biopsy specimens) or their exhaled breath, and;
  • their information (in individually identifiable, re-identifiable or non-identifiable form) as part of an existing published or unpublished source or database being accessed.

At Curtin, ethics applications are submitted and managed through a platform called InfoEd. Curtin Staff and Students can log in using the Curtin Single Sign On (SSO) to access the application platform, as well as information and user guides on using the system, via the Help drop down menu.

These pages have been designed to provide guidance on the Human Ethics processes at Curtin. If you have any suggestions or feedback, please feel free to email us.

Curtin research staff are also required to complete the Research Integrity Training module through iPerform.

Higher Degree by Research (HDR) students are required to complete the Research Integrity and HDR Essentials through Blackboard*

We host Drop-in Sessions during semesters where you can come along and speak to one of our team about anything ethics related. If you would like to speak to one of our friendly team for assistance with your ethics application, you can book an appointment for an in-person or Microsoft Teams meeting via our Bookings page.

Ethics applications

What you need to know about applying for ethics approval from who needs ethics approval, risk categories, supporting documents, approval time frames, and HREC committee meetings and more!

Reporting requirements

Once you have received approval, there are requirements for annual progress reporting, notifying us of changes to your research, and when your research has completed – find out more here.

Help and resources

Handy information including links to policies, FAQs and more

Clinical Trials

Curtin uses the WHO / ICMJE 2008 definition of a clinical trial. That is, any research study that prospectively assigns human participants or groups of humans to one or more health related interventions to evaluate the effects on health outcomes.

For assistance in designing and conducting clinical trials please contact ROC-clinicaltrials@curtin.edu.au or +61 8 9266 9292

Drop in sessions

Drop in sessions

Whether you’re preparing an ethics application, navigating InfoEd or have questions about the research ethics process, the Research Office Ethics Team is here to help.

When: 

  • Tuesdays, 11am
  • Wednesdays, 1pm
  • Between weeks 4–14 (11 August–21 October 2026) – Please note, there are no sessions on September 29 and 30.

Where: Graduate Research School, Building 101, Level 1 (Public entrance opposite Curtin Health Services)

If these times don’t suit, or if you would like a Teams meeting, you can book an appointment with the Ethics team!

Contact the ethics team