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Section 5: For clinical trials investigating a drug and/or device
Guidance on required documentation, agreements, indemnities and Clinical Trial Notification processes for drug and device clinical trials at the Royal Melbourne Hospital.
https://thermh-prod.thirststudios.io/research/office-for-research/research-governance/submit-a-governance-application-for-site-specific-authorisation/section-5-for-clinical-trials-investigating-a-drug-and-or-deviceSection 1: Mandatory components for all SSA submissions
All components in section 1 are mandatory and must be completed for all submissions.
https://thermh-prod.thirststudios.io/research/office-for-research/research-governance/submit-a-governance-application-for-site-specific-authorisation/section-1-mandatory-for-all-ssa-submissions