Veeva Product Surveillance
Maintain a High Standard of Product Quality at All Times
Global product surveillance simplified
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.
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.