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Featured Content

How Sites and Sponsors are Collaborating to Move eSource Forward
On-demand Webinar

How Sites and Sponsors are Collaborating to Move eSource Forward

Explore how collaborative initiatives are shaping eSource implementation, enhancing data integration between clinical sites and study sponsors.
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How to Engage Your IRB to Improve Clinical Trial Risk Management
On-demand Webinar

How to Engage Your IRB to Improve Clinical Trial Risk Management

Learn how IRBs contribute to risk reduction in clinical trials by leveraging their unique oversight to improve data quality and participant safety.
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Navigating sIRB Complexities: An Interactive Session
On-demand Webinar

Navigating sIRB Complexities: An Interactive Session

Watch this recorded webinar as IRB experts address common sIRB challenges, share strategic priorities, and answer questions on preparing for sIRB mandates.
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Real-World Evidence: What Researchers Must Know
On-demand Webinar

Real-World Evidence: What Researchers Must Know

Experts Rebecca Miksad and Tim Stoddard of Flatiron Health provide a practical look at the role of real-world evidence (RWE) in regulatory, drug development, and clinical decision-making.
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