Veeva Product Surveillance | Postmarket Incident Reporting Management

Veeva Product Surveillance

Maintain a High Standard of Product Quality at All Times

Global product surveillance simplified

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QualityDocs QMS Training Product Surveillance
Launched 2020
Status EARLY
Customers 5-10

Harmonize global postmarket surveillance for device products

Veeva Product Surveillance simplifies and standardizes postmarket incident reporting management for medical devices and diagnostics, improving product safety, reliability, and quality.

Seamless connection with quality and regulatory processes enables proactive complaints handling, accelerating continuous innovation throughout the product lifecycle.

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Veeva Product Surveillance Dashboard

Why Veeva Product Surveillance

Simplify and standardize global product surveillance

  • Improve product quality and patient safety

    Proactively identify and resolve product quality issues for greater reliability, safety, and compliance.

  • Ensure submission timeliness

    Meet submission timelines with an intelligent, global reportability decision tree with country-specific criteria.

  • Real-time visibility and end-to-end control

    Make informed business decisions with real-time visibility into submissions and complaint-handling metrics.

RESOURCES

Explore and learn

Are modernized quality applications a predictor of global medtech growth?
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Cardinal Health drives proactive quality management leveraging Veeva Quality Cloud
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Simplifying postmarket surveillance: Introducing Veeva Product Surveillance
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Interested in learning more about how Veeva can help?

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