Verantos Announces Commercial Availability of Regulatory-Grade EHR-Based Study Solution

Real-world-evidence firm helps biotechnology and pharmaceutical companies run observational studies for regulatory and reimbursement support

Verantos, the market leader in regulatory-grade electronic health record (EHR)-based studies, today announced commercial availability of its turnkey solution for real-world-evidence (RWE) study implementation. With the help of Verantos, biotechnology and pharmaceutical firms can run highly accurate observational studies appropriate for regulatory and reimbursement support.

Verantos, the only RWE firm providing regulatory-grade EHR-based study technology, designed a framework to leverage both structured and unstructured EHR data for optimal clinical insight. The firm uses artificial intelligence (AI), including natural language processing and machine learning, to generate highly accurate RWE. This enables Verantos to run studies on difficult inclusion criteria, exposures, and outcomes that would otherwise be inaccurate or impossible. The turnkey solution provided to biopharmaceutical clients includes study protocol, data licensing, technology implementation, independent cohort validation, study completion, and publication of regulatory-grade observational studies.

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“The key to EHR-based study validity is sufficient data accuracy and generalizability to support the clinical assertion,” said Dan Riskin, MD, MBA, Founder and CEO of Verantos. “Verantos technology leverages rich data sources, enhances cohort accuracy, and ensures demonstrable study accuracy. We see a growing market demand for regulatory-grade studies based on regulatory agencies and health plans increasingly expecting proof of data validity in EHR-based studies.”

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