Automating pharmacovigilance to increase efficiencies.

The proliferation of new data sources is increasing opportunities to validate your product's safety. But resource pressures and expanding regulatory requirements makes pharmacovigiliance hard to scale. IQVIA can help.
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Combining technology and analytics with expertise

IQVIA's safety teams are harnessing the power of automation, artificial intelligence (AI) and machine learning to design, build and execute end-to-end safety solutions.

And as one of the world's largest pharmacovigiliance organizations, IQVIA brings extensive domain expertise and deep regulatory intelligence to every program.

Pharmacovigilance: Innovate to automate

Our flexible, global delivery models are delivered via leading-edge technology platforms, enabling predictable, quality delivery across complex multi-year programs. High impact improvements include

  • Automating safety case processing to improve efficiencies while increasing quality and productivity
  • Auto generation of patient narratives and machine translation of documents and images into usable formats
  • Identification of Adverse Events (AEs) highlighted in online or mobile communications to improve safety reporting capabilities

IQVIA is leading the charge in leveraging artificial intelligence and smart machines to identify, ingest, and report out safety signals in structured and unstructured data.


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Navigate complex regulatory requirements with expert insights and bring transparency, efficiency and predictability to your regulatory affairs strategy.

Regulatory Compliance

Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.

Commercial Compliance

Partner with compliance experts to create, implement and manage efficient, end-to-end processes that ensure your organization is compliant with global engagement and transparency regulations and codes.

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