Our team of pharmacovigilance specialists leverage technology to deliver global case management for clinical and post-marketing products.
Manage high volumes of safety reports efficiently
Standardized workflows enabled by automation tools to streamline processes and increase efficiencies.
Standardize Global Data
Centralized solution to process data from multiple intake formats, resulting in a highly compliant output.
Generate meaningful safety insights, faster
Best-in-class technology and people to increase availability of well-coded data and drive faster, more meaningful signal management.
End-to-end case management
Integrated Medical information
Digitally enabled intake
Facilitate digital and analogue intake across multiple channels through a unified solution that drives standardization and compliance.
Accurate and compliant reporting
Timely reporting of outbound ICSRs meeting the highest standards of regulatory expectations along with efficient compilation of aggregate reports.
Enhanced case processing
Leverage technology to standardize safety reports and reduce errors, enabling pharmacovigilance experts to focus effort where it matters most.
Expert medical review
Expert assessment focused on the individual cases that matter most, enabling targeted follow-up and rapid downstream signal detection.