Gain a comprehensive understanding of the latest advancements and regulatory updates in RWE from leading experts in the field
Engage with industry leaders, regulatory authorities, and peers to discuss innovative strategies and practical applications in RWE
Explore diverse use cases and methodological insights across early development, late-phase, and post-marketing scenarios to enhance your knowledge and practice
Discover cutting-edge technologies and operational strategies that are shaping the future of RWE generation
Examine the intersection of AI and RWE, and discuss the implications for policy and regulatory frameworks
Stay at the forefront of real-world evidence (RWE) with the latest advancements, regulatory updates, and practical applications from leading experts and key industry players
Deep dive into various stages of drug development, from early-phase studies to post-marketing safety, and understand how RWE is applied across different use cases
Learn about the latest methodological approaches and innovations in RWE, including causal methods, negative control outcomes, and sensitivity analyses
Discover new technologies and operational strategies that enhance RWE generation, such as AI-enabled data abstraction and data linkage techniques
Explore strategies to address health equity and improve diversity in drug development, leveraging RWE to build more representative and inclusive study populations
Gain insights into international regulatory perspectives and practical challenges in using RWE, and learn how to balance data innovation with scientific rigor
Understand how artificial intelligence is transforming clinical study designs and policy frameworks, and explore the future intersection of AI and RWE in pharmacoepidemiology
Case Study Spotlights
From concept to execution, each spotlight offers a deep dive into the design process, outlining how we tackle complex challenges and deliver measurable success.
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