Forms and templates - NALHN research applications
The Research Governance Office (RGO) appreciate that there are many supporting documents required in the preparation and ongoing management of research projects. The following checklists and cover sheets are useful when submitting an application.
Checklists/Guides
- NALHN RGO Submission Checklist (DOCX 71KB) –Summary of all requirements, bank details, contractor details etc
- Confidentiality Agreement Checklist (DOCX 82KB) - For sharing sensitive information prior to a study.
Forms
- RGO Fee Form (DOCX 32KB)
- NALHN Confidentiality Deed non-NALHN Employee (DOCX 32KB)
- NALHN Clinical Trial Study Team Declaration Form (PDF)
- Research Coordinator Authorisation Form (DOCX 68KB)
- NALHN Research Data Management Plan (DOCX 401KB)
Templates
- NALHN Standard of Care Radiation Certification (DOCX 22KB)
- Research Protocol Template (DOCX 63KB)
- Low-risk Research Protocol Guideline (DOCX 31KB)
- Budget Staff Divisional contribution In-Kind services NALHN (XLS 13KB)
- NALHN Research Quality Assurance template (DOCX 82KB)
Participant Information and Consent Form (PICF)
For commercial studies, the lead site will usually provide you with an ethics approved Master PISCF, and you’ll update that to a Site Specific PISCF. But if NALHN is the lead site, then you’ll need to access the NHMRC’s PISCF consent forms.
All PISCF forms require the up to date the version control in the document footer.