Our research and funding documents contain support and reference information for applicants applying for funding, as well as background information for referees and committee members.
This example Memorandum of Understanding (MoU) formalises the intention of the parties to collaborate in a research project and to enter into a sub-contract.
The HRC is responsible to the Minister of Health, and its major funding agreement is through the Minister of Science and Innovation. Our statutory functions are outlined in the Health Research Council Act 1990.
This CV template, used by several other organisations, can be used in all HRC funding applications. It standardises the type of information asked for and eliminates the need for researchers to reformat their CV each time they apply for funding.
The HRCEC requires ethics committees to provide an Annual Report from an Ethics Committee, which allows the HRCEC to monitor the activity and functioning of the committee.
The Health Research Council's Standing Committee on Therapeutic Trials (SCOTT) undertakes scientific assessment of applications to conduct trials and makes recommendations to the Director-General of Health on whether or not trials should be approved.
The Data Monitoring Core Committee (DMCC) was established to provide objective, independent monitoring of clinical trials funded by the HRC. This flow-chart explains the process.
The primary function of the Data Monitoring Core Committee (HRC DMCC) is to ensure that HRC-funded trials that require data and safety monitoring are adequately monitored.
Criteria for trials that require data and safety monitoring: