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CIRB LOCAL SERIOUS ADVERSE EVENT (SAE)REPORTING Formal sections must be completed. Principal Investigator: Designation Department: Institution: Text Field CIRB Reference No: Protocol Title (as per
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CIRB local serious adverse refers to serious adverse events that occur during a clinical trial.
The principal investigator or sponsor of the clinical trial is required to file CIRB local serious adverse.
CIRB local serious adverse can be filled out online through the designated platform provided by the Institutional Review Board.
The purpose of CIRB local serious adverse is to ensure the safety and well-being of clinical trial participants by promptly reporting any serious adverse events.
Information such as the nature of the adverse event, date of occurrence, severity, actions taken, and follow-up should be reported on CIRB local serious adverse.
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