SOP for Pharmacovigilance Adverse Event (AE) Reporting
SOP for Pharmacovigilance Adverse Event (AE) Reporting Guidelines for Pharmacovigilance Adverse Event (AE) Reporting 1) Purpose The purpose of this SOP is to outline procedures for the reporting of adverse events (AEs) associated with pharmaceutical products. 2) Scope This SOP applies to all pharmacovigilance personnel responsible for AE reporting, including pharmacovigilance managers, safety scientists, and…
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