Making the Grade: Registries as Sources of Regulatory-Grade RWE
When executed with precision, protocol-driven registries provide invaluable real-world data (RWD) and real-world evidence (RWE) that can power diverse research initiatives — ranging from safety studies to comparative effectiveness research.
Yet, choosing the right registry isn’t always straightforward. With a variety of registry types and differences in data quality, granularity and ownership, it can be a challenge to ensure you’re selecting a resource that meets your long-term research needs.
In this article, uncover key insights, including:
- Types of clinical registries: Understand the differences between single-sponsored, multi-sponsored and independently-sponsored registries and how each impacts your research approach.
- Key data collection: Learn about the essential clinical, safety and patient-reported outcome (PRO) measures required to produce regulatory-grade RWE.
- Best practices for registry selection: Gain insights on navigating critical factors that impact registry selection, including scale, evidence credibility, data completeness and long-term follow-up needs.
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