IQVIA Vigilance Intake

Innovating Intake.

Rethink case intake and imagine an optimized, unified process that addresses the challenges of growing data volume, complexity and quality through the use of automation and AI. 

IMPROVE YOUR DATA QUALITY
How ready is your safety data?
Manual data entry has a dramatic impact on data quality. A recent analysis of 5,000 new cases for a large pharmaceutical company revealed 50% contained data that did not match their unstructured narratives. 10% to 20% of these cases were fundamentally incorrect.*

Take advantage of our offer to diagnosis the health of your cases.

Intake demands continue to grow

Challenged with managing increasing volumes of adverse events, pharmacovigilance organizations are constrained by limited resources and outdated technologies while facing mounting compliance expectations from regulatory agencies.

New ways to manage data receipt, storage and analysis.

Streamline intake of your safety information by leveraging AI, ML and NLP to automate the receipt of adverse events.

  • Transform key activities such as case validation, duplicate check and redaction
  • Look beyond traditional intake functions and consider downstream challenges that occur during case processing

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