A Patient Insights Network (PIN) is much more than a traditional registry. It’s a powerful tool for collecting, curating, coordinating, and delivering patient data.
So far, we’ve established PINs for more than 400 specific medical conditions—and counting. Our team, which began as PatientCrossroads, has years of expertise that shapes our approach. We have worked with the National Institutes of Health (NIH), the Patient-Centered Outcomes Research Institute (PCORI), numerous biopharma companies, and scores of advocacy organizations.