Qld Health Research Management Policy (QH-RMP) Queensland Legislative Requirements Researcher User Guide (RUG) Access to Confidential Health Information held by Qld Health Review and approval of QA/Clinical Audits Uniform Requirements for Manuscript Submission Central Coordinating Service Fees and Site Information for Commercially Sponsored Research Standard Fees For Industry Sponsored Research GCP Standard Operating Procedures (SOPs) for clinical research Coordinating Principal Investigator Guidance for Multi Centre Research Commercially sponsored Investigator initiated
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Strategic Principles for a National Approach to Australian Clinical Quality Registries
Note
The 'Word' version of the Low and Negligible Risk Form has been removed and previously downloaded copies will be accepted by HRECs until the end of April 2012. Any extensions will need to be negotiated with HRECs.
Access the NEAF and Low and Negligible Risk Form Where Do I Submit My Single Site Research Study For Ethical Review? How do I submit my Multi-centre Research Study for Ethical Review? Access To Tissue Samples Held By Qld Health (CaSS) Use of Anatomical Pathology Specimens for Research Queensland Civil & Administrative Tribunal Forms (QCAT) Standard Reporting Forms HREC and RGO Fees for Industry Sponsored Research
Site Specific Assessment (SSA) Guidance & Sample Forms Where do I submit my SSA Form for RGO Review
Medicines Australia Clinical Trial Agreements (CTAs) Medical Technology Association of Australia Qld Health Intellectual Property (IP) Schedule 7 Clauses Approval process Review template Companies with preapproved Clauses Qld Health Contract Signing Delegations Clinical Trials Agreements Guidelines and Advice
Last Updated: 26 July 2011 Last Reviewed: 26 July 2011
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