For single centre research projects the Co-ordinating Investigator must provide reports of adverse events to the HREC that approved the project.

For multi-centre research projects the Principal Investigators must report serious adverse events (SAEs) and suspected unexpected serious adverse reactions (SUSARs) occurring at the site directly to the lead HREC that approved the project. The Principal Investigator must also provide a copy of these reports to the Research Governance Officer and Co-ordinating Investigator. All other safety reports must be submitted to the lead HREC that approved the project by the Co-ordinating Investigator. 

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