Our policy documents guide our decision making and behaviour. They outline the steps and actions we need to take for ethical and responsible research in Metro South Health.
Research excellence
Research support and management
| Document name and number | Documents |
|---|---|
PR2023-412 Research support and management |
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WI2023-293 Research funding, budgets and infrastructure support |
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WI2022-226 Open access journal publications in research |
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WI2023-294 Research grants administration |
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WI2023-295 Research letters of support |
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WI2023-296 Metro South Health Research Support Scheme (MSHRSS) |
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WI2023-297 Gift cards (for use as research incentives) |
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| WI2023-298 Scientists in the Clinic program (MSH/TRI) |
Research administration and compliance
| Document name and number | Documents |
|---|---|
PR2023-413 Research administration and compliance | |
WI2023-299 Ethical and scientific review of research |
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WI2023-300 Exemptions from research review |
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WI2023-301 Site specific assessment of research | |
WI2023-302 Research contracts and study execution | |
WI2023-303 Metro South Health sponsorship of Clinical Trial Notification (CTN) scheme trials | |
WI2023-304 PowerTrials - ieMR research support module |
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WI2023-305 Research monitoring |
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WI2023-306 Post approval - research amendment, reporting and closure |
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GL2023-99 Planning a research project |
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GL2023-100 Research Participant Information and Consent Form (PICF) | |
GL2023-101 Research contract clauses |
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GL2023-102 Use of electronic signatures in research contracts |
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GL2021-77 Clinical trials |
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GL2023-103 Teletrial Support Program (TSP) funding |
Clinical Research Facility (CRF)
| Document name and number | Documents |
|---|---|
PR2024-453 Clinical Research Facility |
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WI2024-335 Clinical Research Facility application and use |
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WI2024-336 Clinical Research Facility participant admission, supervision and clinical management | |
WI2024-337 Clinical Research Facility investigational product management and administration | |
WI2024-338 Clinical Research Facility adverse event and clinical incident reporting | |
WI2024-339 Clinical Research Facility laboratory and alarm management |
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WI2024-340 Clinical Research Facility archiving of clinical trial documents |
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