Skip to main content

Read more
Governance Annual Snapshot Reconciliation Action Plan Disability Access and Inclusion Plan Diversity and Inclusion Action Plan Professional Accountability Program Research office Researchers and sponsors Research participants Clinical trials Grants and funding News and events Clinical Strategy Strategic Ambition Consumer Strategy Aboriginal Employment Strategy Research Strategy Concerns about your care Informed consent Consumer experience Consumer partnering Compliments and complaints Your rights as a patient
Careers News Contact us
Governance Annual Snapshot Reconciliation Action Plan Disability Access and Inclusion Plan Diversity and Inclusion Action Plan Professional Accountability Program Research office Researchers and sponsors Research participants Clinical trials Grants and funding News and events Clinical Strategy Strategic Ambition Consumer Strategy Aboriginal Employment Strategy Research Strategy Concerns about your care Informed consent Consumer experience Consumer partnering Compliments and complaints Your rights as a patient

Post approval monitoring

Information and forms for progress reports, safety reports and amendments.

On this page

In accordance with the National Health and Medical Research Council (NHMRC) National Statement on Ethical Conduct in Human Research 2023 those responsible for the oversight of research and monitoring include:

  • researchers
  • institutions
  • reviewing Human Research Ethics Committees (HREC)
  • sponsors.

CALHN is required to monitor all research from project approval to completion.

Monitoring

Post-Approval Monitoring Submissions
Progress Report
Final/Site Closure Reports
Amendments
Serious Breaches, Suspected Breaches and Deviations
Safety Reporting

This page was last updated 9 May 2025.

Back to top