Resource Library

Learn how Prevail InfoWorks helped a sponsor avoid a clinical hold by using the realtime data reporting of The Single Interface™ to prove an issue was not caused by the drug.

Learn how Prevail InfoWorks opens the door for sponsors, investors, and pharma to see clinical trial data in realtime for due diligence as the study is ongoing and earlier transactions.

Learn about Prevail InfoWorks' history of pharmacovigilance breakthroughs, including a recent successful submission on behalf of a sponsor into the FDA's new limited access testing environment for SUSARs.

Prevail’s patented system supports your business development strategies

Our innovative and modular safety system makes safety and risk management easy, compliant, and affordable for any life sciences company.

Prevail’s patented RTSM technology platform delivers fast, accurate, and controlled randomization and trial supplies management while keeping your budget in check.

Prevail’s eTMF provides a paperless and automated system for collecting essential documents, while helping identify gaps and manage workflow processes across multiple team members and functional groups in real-time.

Discover how researchers with timely, direct access to high-value visualizations and early observations across every aspect of their studies were able to achieve the first-ever FDA approval in a challenging indication – while saving time, effort, and cost.

Prevail’s innovative analytics provide timely, data-driven insights into live studies, regardless of protocol, data, and system complexity – all without breaking the blind. Improve study success with early observations of aggregated data across your studies and programs.