Review the full scope of population grouping impact

Reference no: EM133406573

Question: A sponsor is evaluating whether they should collect the adverse events (AEs) occurring in clinical trial or review the full scope of population grouping impact. Reason being, the patient population pooled for a therapeutic indication study is within the age bracket that could potentially have other underlying medical conditions. Provide your strategy for AEs reporting.

Reference no: EM133406573

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