By linking clinical trial data to real-world data, clinical research sponsors can have never before available insight into their clinical trial subjects’ disease progression. The linked data can help sponsors answer questions from regulators and position sponsors for post-marketing reporting.
In this discussion, join experts from Parexel, Datavant, and Janssen to learn more about how to effectively implement real-world data linking for clinical research, registries, post-marketing requirements, and more.
Learn how to safely and securely link data with HIPAA and GDPR consideration as well as examples of real-world application in data linking. We’ll cover specific studies that have leveraged linking technology to source patient-level data in a compliant, secure, and patient-centric way.