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Verantos to Present Practical Approaches in High-Validity Real-World Evidence Generation at ISPE’s 41st Annual Meeting

Approach to fit-for-use real-world data grounded in peer-reviewed, published methods, and industry collaboration

Verantos, the global leader in high-validity real-world evidence at scale, announced today that it will present practical approaches for generating high-validity real-world evidence (RWE) at the International Society for Pharmacoepidemiology (ISPE) 41st Annual Meeting in Washington, D.C.

CEO Dan Riskin will share approaches to achieve fit-for-use RWD based on real-world learnings from large pharma collaborations and the FDA-sponsored Verantos-led TRUST and VERIFY studies. He will discuss “Data reliability: implementing accuracy, completeness, and traceability in practice.”

“The goal isn’t just to measure data reliability; it’s to optimize it and to do so using peer-reviewed, published methods so metrics can’t be gamed,” said Riskin. “Evidence generated using low-quality or untested RWD remains suspect as it always has been.”

Symposium snapshot

  • ISPE 41st Annual Meeting, Washington, D.C.
  • Real-world evidence fit for regulatory applications — what does good look like?
  • Tuesday, August 26, 10:30am EDT

Verantos will detail practical implementation approaches to quantify and improve accuracy, completeness, and traceability consistent with peer-reviewed methods and learnings from the TRUST and VERIFY studies. Early findings from this work have been published in JAMA Network Open, providing a transparent foundation for reliability measurement and optimization.

About Verantos

Verantos is the global leader in high-validity real-world evidence for life sciences organizations. By incorporating robust clinical narrative data and artificial intelligence technology, Verantos is the first company to generate high-validity evidence at scale across therapeutic areas with measured accuracy, completeness, and traceability. Credible evidence accelerates clinical development, market access, medical affairs, pharmacovigilance, and regulatory initiatives.

The goal isn’t just to measure data reliability; it’s to optimize it and to do so using peer-reviewed, published methods so metrics can’t be gamed.

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