Introduction to Veeva Vault Safety
Veeva Vault Safety, a cutting-edge individual case safety report (ICSR) management system, revolutionizes adverse event management for clinical and post-marketed products. This modern solution offers seamless support for the intake, processing, and submission of adverse events on a global scale.
Streamlined Global Adverse Event Processing
Within Veeva Vault Safety, sponsors and Contract Research Organizations (CROs) can efficiently process global and domestic adverse events related to drugs, biologics, vaccines, devices, and combination products. The system provides built-in gateway connections and reporting rules that streamline the management of case submissions to health authorities and distribution to partners.
Centralized Coding Dictionary Management
Veeva Vault Safety simplifies adverse event coding with automated management of coding dictionaries. This includes semi-annual updates for MedDRA, WHODrug, and EDQM, ensuring that sponsors and CROs maintain compliance with the latest standards and classifications.
Key Features and Benefits of Vault Safety
Vault Safety offers numerous advantages, such as streamlining adverse event management processes, automating intake through submissions, ensuring end-to-end safety processes, providing global case view and oversight, and facilitating compliance with new regulatory requirements through regular updates. Customers can leverage these features to enhance safety oversight, improve case processing efficiency, and stay ahead of evolving industry demands.
Customer Success Stories
Veeva Vault Safety has enabled organizations like Merck to streamline their processes and achieve unified safety oversight. Customer testimonials highlight the system's user-friendly nature, seamless integration, and intuitive design, emphasizing the transformational impact it has had on pharmacovigilance operations.
Resources and Further Learning
For those interested in learning more about Veeva Vault Safety, a range of resources are available, including blog posts, articles, case studies, and videos. These materials provide insights into optimizing safety data control, transforming pharmacovigilance practices, and leveraging safety intelligence to enhance patient safety.
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