The use of real-world evidence (RWE) in drug development has been fueled by an increased acceptance of RWE by stakeholders such as regulatory agencies, health technology assessment bodies, and payers, as well as a plethora of real-world data (RWD) sources.
Discover how protocol-driven disease registries—purpose-built for research—serve as one of the most clinically rich sources of real-world data (RWD). Explore how these registries are used to efficiently fulfill post-approval safety commitments, monitor treatment patterns, and describe the natural history of diseases, while uncovering best practices for selecting the right registry for your research needs.
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