Veeva Vault Product Surveillance
Simplifying and standardizing global post-marketing studies! Accelerating continuous innovation.
This product is an application that simplifies and standardizes post-market surveillance of medical devices, improving the safety, reliability, and quality of the products. Rapid reporting of adverse events is ensured through fully automated electronic reporting to authorities and the output of written submission documents. Seamless integration with quality and regulatory processes enables proactive complaint handling throughout the entire product lifecycle, accelerating continuous innovation. 【Features】 ■ Global reporting obligation determination tree ■ Reporting deadline management ■ Automated adverse event reporting ■ Interactive dashboard and reports ■ Customizable adverse event management workflow ■ Part of Veeva Vault Quality Suite *For more details, please refer to the PDF materials or feel free to contact us.
- Company：Veeva Japan
- Price：Other
