Providing science-led, regulatory grade real-world evidence and clinical insights on post approval safety and effectiveness of novel therapies. Offering syndicated registry data and analytics, patient experience and insights, precision medicine solutions, and specialty EMR and claims data. Powering the life sciences industry with the most objective clinical insights. Our data have been used in hundreds of peer reviewed manuscripts and abstracts. We conduct active safety surveillance to support regulatory commitments for new drug approvals, including formal post authorization safety studies.