Simplify and standardize global product surveillance
Launched 2020
Status Early
Customers 1-10
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.
Veeva Product Surveillance Impact
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.Gain real-time visibility and end-to-end control
Make informed business decisions with real-time visibility into submissions and complaint-handling metrics.
Customer Success
Medtechs unify quality management with Veeva Quality Cloud
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TOSOH drives product safety, supports business growth, and informs smarter decision-making.
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Alcon and Merit Medical share their strategies for unlocking AI's potential in regulatory & quality
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Philips and Eli Lilly discuss how the role of quality must change and expand
