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Streamline Clinical Serious Adverse Event (SAE) Reporting and Management Benefits

Streamline Clinical Serious Adverse Event (SAE) Reporting and Management Benefits

Veeva
Pages 2 Pages

Veeva's Safety-EDC Connection streamlines clinical SAE reporting by automatically exchanging comprehensive event data—including over 200 casebook/custom fields (doubling E2B)—between data management and pharmacovigilance teams. This reduces site queries, accelerates case processing, enhances safety output quality, and provides visibility into SAE receipts and case IDs when promoted in Veeva Safety, enabling faster reconciliation and collaboration.

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