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Understanding the Benefits of Data Registries for Advancing Patient Centricity and Research

Electronic Health Reporter

By Leon Rozenblit, JD, PhD, Registry CoE, IQVIA, Alexandra Weiss, nonprofit strategy, patient organizations, IQVIA. This article is copyrighted strictly for Electronic Health Reporter. Illegal copying is prohibited.

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Cultivating an Early Warning System in Healthcare Quality Through Bi-Directional Patient-Physician Engagement 

HIT Consultant

Patient advocacy organizations and medical specialty societies can serve as a liaison between patients and providers in bi-directional engagement, closing gaps in the patient journey and ultimately driving innovation for higher quality care. The 21 st Century Cures Act is enabling patient-driven healthcare information exchange.

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Creating A Thriving Patient-Centric Data Economy

HIT Consultant

Anne Kim, co-founder and CEO of Array Insights We shouldn’t underestimate the power of patient data. Every data point from clinical studies and patient medical records provides fuel for researchers. As we sit here today, the research ecosystem isn’t working to its full potential.