Can a Pharmacovigilance professional work in clinical research organizations (CROs)?
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1 Answer
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Yes, Pharmacovigilance professionals can work in clinical research organizations (CROs), as these companies conduct clinical trials and monitor drug safety.
In CROs, pharmacovigilance specialists analyze adverse events, ensure regulatory compliance, and contribute to clinical trial data integrity. Their role is crucial in maintaining drug safety during pre- and post-marketing phases.
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