Streamlining Postmarket Incident Reporting
Veeva's Vault Product Surveillance (VPS) software offers a comprehensive solution to simplify and standardize postmarket incident reporting management for medical devices and diagnostics. By harmonizing global postmarket surveillance practices, VPS empowers organizations to maintain a high standard of product quality across geographies.
Enhancing Product Safety and Reliability
Through seamless integration with quality and regulatory processes, VPS enables proactive complaints handling, facilitating continuous innovation throughout the product lifecycle. By proactively identifying and resolving product quality issues, companies can enhance product safety, reliability, and compliance.
Ensuring Submission Timeliness and Compliance
VPS includes an intelligent, global reportability decision tree with country-specific criteria, ensuring timely submissions of postmarket incident reports. By meeting submission timelines consistently, organizations can demonstrate compliance with regulatory requirements and industry standards.
Real-time Visibility and Informed Decision-Making
With Veeva Vault Product Surveillance, companies gain real-time visibility into submissions and complaint-handling metrics, empowering them to make informed business decisions. This transparency and end-to-end control over product surveillance processes contribute to operational efficiency and regulatory compliance.
Empowering Medtech Growth and Innovation
By leveraging VPS to simplify postmarket surveillance, organizations can allocate more resources to driving growth and innovation in the global medtech industry. Veeva's modernized quality applications serve as a foundation for proactive quality management, enabling companies like Cardinal Health to enhance product quality and patient safety effectively.