Standardizing Clinical Data for Safer, Faster Drug Approvals

Our Chief Medical Officer, Jose Galvez, shares his background from the FDA and NIH, and why data standards are so critical for clinical research. He explains how frameworks like FHIR and the USCDI create a baseline of interoperable EHR data—helping sponsors, clinicians, and regulators ensure safety and efficacy decisions are made with trusted, consistent information.

From cardiology trials to oncology studies, standardized measures like heart rate, EKGs, and lab values play a vital role in turning everyday clinical data into reliable evidence for trials.
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