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At Ramsay Health Care, all research projects conducted in Australia must undergo ethical review and approval in accordance with the National Statement on Ethical Conduct in Human Research (2023) and Ramsay’s facility rules.

Approval process

Before beginning research at a Ramsay Health Care facility, the Researcher must secure:

Research Endorsement
  • Researchers must obtain a signed Research Endorsement Form from the relevant site executive prior to registering their project in REGGS and submitting the ethics and/ or governance application.
Ethics approval
  • Granted by a Ramsay Human Research Ethics Committee (HREC) or another HREC certified by the National Health and Medical Research Council (NHMRC).
  • The approval letter must list all Ramsay facilities and any external sites involved in the research.
Research Governance approval
  • Issued by the CEO of the Ramsay facility following a governance review by Ramsay Health Care.

Applying for ethical review

Ramsay’s Human Research Ethics Committee (HREC) reviews ethics applications for:

  • Research conducted in Ramsay hospitals by accredited practitioners or employees.
  • Low or negligible risk research in co-located practitioner rooms.
  • Applications from students enrolled in University Programs must be submitted for review and approval by the respective University HREC. If a Ramsay Health Care facility is involved in the study, the facility name must be listed in the approval letter and a request for reciprocal review must be submitted to Ramsay Health Care HREC.
 
Ramsay Health Care HREC

Ramsay operates one HREC in compliance with the National Statement on Ethical Conduct in Human Research (2023):

  • Ramsay Health Care Human Research Ethics Committee A

This committee includes diverse representatives, such as medical practitioners, researchers, legal experts, clergy and community members.

Please note that the Ramsay Health Care WA|SA HREC will be closing effectively 5th May 2026, and the ethical oversight will be transferred to the HREC A.

Contact

Meeting dates

Ethics fees

Research types and processes

Low-risk studies

Higher-risk studies

Case report

Quality audit (QA) and quality improvement (QI)

Authorised prescriber scheme

Post-approval management

Changes to approved research

Progress reporting

Safety reporting

Breaches of protocol

Complaints

Study participants

Researchers

Visit our resources page to find out more

Ethics resources

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