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Researchers and sponsors

Safety, quality and compliance are vital in research, and at CALHN we ensure all criteria are met to reduce risks and protect privacy and confidentiality for consumers and staff.

Tick all the boxes

CALHN research adheres to strict regulatory frameworks, ethics and governance approvals.

Our Research Services Office provides support to researchers and sponsors in research governance (including for clinical trials), ethics committee submissions, finance, quality assurance, safety, monitoring, publication and more. We also provide templates for investigator site file documents.

National Clinical Trials Governance Framework (NCTGF)

A comprehensive set of guidelines to ensure clinical trials are conducted in a safe and high-quality environment for patients and the community.

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Human Research Ethics Committee (HREC) submissions

Learn more about CALHN HREC and its approval processes

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Research governance

CALHN research governance details and submissions.

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Clinical trials for researchers

Learn more about commercially sponsored clinical trials by accessing agreements, guides and governance requirements.

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Low risk project submissions

Information and forms for low risk submissions

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Quality assurance quality improvement and audits

Information and requirements for quality assurance (QA), quality improvement (QI) and audit activities

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Post approval monitoring

Ensure you are up to date with mandatory progress reporting, safety reporting and amendments

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Education and training

Education and training opportunities at CALHN

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Grants and funding

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Research finance

Information and guidelines for research finance

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Investigator site file document templates

Essential documents that are mandated for ensuring study compliance across all investigator initiated and sponsored clinical trials

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Clinical trials

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ClinTrial Refer

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RAH research publications

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TQEH research publications

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