Clinical Trials Network
Improving Australians access to the latest prevention and treatment trials
The NACE Clinical Trials Network is a one-stop-shop to help fast-track the start-up of national allergy trials. It is building trial-ready capacity across Australia by supporting allergy triallists and sponsors with:
- National site identification for trial start-up and operation
- Budget guidance to ensure sustainable programs across multiple sites
- Connections to relevant collaborators via the NACE membership of almost 500 allergy experts, and beyond
- Practical resources such as templates, ethics submission guidelines, trial start-up checklists, and more
- Onboarding new staff, including access to relevant resources
- Trial promotion on the NACE Allergy Studies Directory
- NACE endorsement of investigator-initiated clinical trials.
Find tools and resources curated to help conduct both investigator-led and sponsored trials.
Interested in how the NACE Clinical Trials Network can support your next allergy trial?
Let us know how the NACE Clinical Trials Network can best help you.
Australian Clinical Trials Alliance
The NACE is an Associate Member of the Australian Clinical Trials Alliance. Visit the ACTA Resources Library for materials that support investigator-led clinical trials.
Australian Clinical Trials Education Centre (A-CTEC)
A member-based education platform, hosting a suite of evidence-based, interactive clinical trials education opportunities suitable for a range of learning needs.
METIS Document Library
A searchable repository of guidance, procedures, and templates to help you conduct research in accordance with Melbourne Children’s, state, national and international legislation and regulatory requirements.
NHMRC research policy
The NHMRC is the key driver of health and medical research in Australia. Visit its comprehensive suite of information and resources related to conducting and translating Australian research.
Ethics and governance
- Research Ethics and Governance – Single Site flow sheet
- Research Ethics and Governance – Process for Lead and Accepting Sites
- Australia New Zealand Clinical Trials Registry – Register your trial
- Responsibilities of Site PI’s for Investigator Initiated Trials: Safety Assessment, Documentation and Reporting
- SOP – Internal Auditing
Protocol templates
- Risk Assessment and Risk Management Tool
- Protocol Template Clinical Trial Protocol (non-drug, non-biological, non-device intervention)
- Protocol Template Observational Studies Protocol
- Protocol Template Clinical Trial Protocol (drug or device intervention)
- Participant Consent, Screening and Enrolment Log
Feasibility guidelines
Trial start-up checklists & audits
In proud partnership with
