902 results found

Streamlined ethics & governance review

RMH entered into a Memorandum of Understanding with 11 partner organisations to streamline and harmonise ethical and governance review of all multicentre human health research.


Approval to work with GMOs

The Gene Technology Act 2000 regulates the use and release of genetically modified organisms (GMO) to protect the health and safety of the public and their environment.


Budget reviews for site specific approvals

Financial management is an essential component of any research project and needs to be included as part of the site-specific application to the RMH.


Good Clinical Practice training

The Good Clinical Practice (GCP) guideline is the international ethics and scientific quality standard for conducting clinical trials


COVID-19 guidance for clinical trials & research projects

The safety and wellbeing of trial participants, other patients, visitors, researchers and other clinical and support staff is paramount.


Research fees & payment schedule

The Office for Research oversees all aspects of research at the RMH, with the major component of work arising from the operation of the HREC and the governance of research projects undertaken at or by the RMH.


Research involving ionising radiation

Researchers proposing to expose research participants to ionising radiation should provide information that allows consent to be properly considered by research participants.


Consent process for research involving people without decision-making capacity

The Medical Treatment Planning and Decisions Act 2016 (Vic) provides a framework for making decisions about medical treatment when people do not have the capacity to make their own decisions.


Research integrity advisors

The RMH's research integrity advisors are a key resource for advice and support with regard to research integrity and misconduct, as well as our processes and procedures relating to research integrity.


REDCap for data collection in research

Research data and metadata must be collected, stored, retained, used and disposed of in a way that protects the rights, safety, and wellbeing of the research participants and wider community. REDCap can help meet these data requirements.

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