Resources

Commercial Sponsors:
- Evaluation of a trial for a Teletrial_guideline_SPO_ v3 Nov 2024
- Evaluation of a site as a Satellite Site_guideline_SPO_v3 Nov 2024
- Ethics Teletrial_checklist_SPO_v4 Feb 2025
- Teletrial RGO Review_checklist_SPO_v2 Nov 2024
- HREC Notification_checklist_SPO_v2 Nov 2024
- Teletrial Budget and Costing_guideline_SPO_v2 Nov 2024
- Satellite Site Workflow Pre Approval_checklist_SPO_v3 Nov 2024
- Satellite Site Workflow Post Approval_checklist_SPO_v2 Nov 2024

**NEW** Teletrial Supervision Plan:
- EDUCATIONAL VIDEO– Learn how health professionals work together to deliver teletrials, under the guidance of the nationally harmonised ‘Teletrial Supervision Plan‘
- EDUCATIONAL VIDEO- See our guidance outlining how to fill in the ‘Teletrial Supervision Plan‘ template. This includes clinical trial details, protocol-specific activities and endorsement
- ATP National Supervision Plan_Updated_v2_07052024

Trial Documents:
- Stand Alone Teletrial Participant Information Sheet and Consent Form (PICF)
- Human Research Ethics Committees
- Guidance for the use of optional Teletrial Wording in PICF templates
- NHMRC PICF templates (see Additional resources)
- Clinical Trial Research Agreement/Clinical Trial Agreement
- Clinical Trial Research Agreement – Tele Trials Subcontract
- MTAA Clinical Investigation Research Agreement