Veeva Vault Product Surveillance
Vault Product Surveillance simplifies and standardizes postmarket surveillance for medical devices, improving product safety, reliability, and quality. Fully automated electronic health authority submissions and non-electronic submission outputs ensure timely adverse event reporting. Seamless connection with quality and regulatory processes enables proactive complaints handling, accelerating continuous innovation throughout the product lifecycle.
- 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.