Pegasystems Adverse Event Case Processing Solution Helps Life Sciences Organizations Improve Operational Efficiency with Increas
New solution shortens timelines and automates reporting compliance for adverse events during clinical trials and post-approval safety monitoring
CAMBRIDGE, Mass. – November 2, 2010–Pegasystems Inc.(NASDAQ: PEGA), the leader in business process management (BPM) and a leading provider of customer relationship management (CRM) solutions, today released its newAdverseEvent Case Processing solution for the Life Sciences market. Built on Pega’s industry-leading Build for Change® technology, this solution revolutionizes how organizations collect, manage and analyze adverse events both during and after clinical trials, thereby shortening the timeline for conducting successful clinical trials and improving the post-approval management of safety information.
All clinical trials and marketed products have the potential to produce adverse events ranging from minor to serious in nature, even when available to the general public. Adverse events categorized as "serious," or something that could result in initial or prolonged hospitalization or death, must be reported to regulatory authorities immediately. In a highly competitive industry where patent expirations and rising drug development costs are pressuring bottom lines, life sciences companies need better operational efficiency to adapt to changing regulations and reduce costs. The Adverse Event Case Processing solution improves various stages of pharmacovigilance operations. New automation and operational efficiencies that leverage built-in business process management capabilities:
This new solution is designed for rapid deployment by using advanced technologies to quickly leverage existing adverse event processing rules and requirements and can produce dynamic, specialized documentation to help ensure compliance in a validated environment.
Quotes & Commentary:
Maryanne Quinn, President, Integrated Submission Strategies, LLC.
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