The core pain point is data paralysis. To combat epidemics, allocate resources, or study health disparities, researchers need granular, individual-level data. However, sharing identifiable health records violates regulations like HIPAA and erodes public trust. This forces agencies to rely on aggregated, delayed, or incomplete datasets, crippling their ability to perform timely, impactful research and model disease spread with accuracy. The business cost is inefficient spending and slower response to public health crises.













