Data Management STREAM

  1. Evolving Data Review With AI 2/25/2025

    AI is transforming clinical data review by automating processes and enhancing efficiency. Discover the four stages of evolution that emphasize automation, regulatory alignment, data analysis, and human oversight.

  2. Partnership That Eases The Path From Discovery To Clinical Trial 4/26/2023

    The path from discovery to clinical trials is filled with unexpected turns, but the right CRO partner dedicated to delivering clinical development solutions can help.

  3. The Importance Of Reliable Data To Clinical Trial Activation 5/8/2025

    Find an easier way to identify and enroll eligible patients for your clinical trials with quality data and site selection.

  4. AI Meets Informed Consent: Opportunity, Risk, And What IRBs Need To See 5/14/2026

    Expert perspectives on IRB oversight, health literacy, and research ethics offer practical guidance to strengthen consent, protect participants, and align compliance with real-world research.

  5. Trialtrove: Clinical Trial Data You Can Depend On 10/13/2021

    Trialtrove’s data, compiled from over 58,000 sources, helps study sponsors and CROs make informed decisions around clinical trial strategy, design, and execution. 

  6. Castor Product Spotlight: The Self-Driving Study 3/17/2026

    Discover how agentic AI automates clinical workflows, reducing data timelines from weeks to hours and cutting chart review costs by 90% while maintaining regulatory-grade rigor and audit readiness.

  7. What Should You Ask The FDA About AI 1/27/2025

    Understanding what some of the common questions the FDA gets about AI may help you as you plan to interact with the agency.

  8. How ICH Oversight And AI Are Shaping The Future Of Clinical Trials 10/9/2025

    Explore how the new ICH E6 (R3) revisions are reshaping clinical trial oversight and examine how AI-driven tools like the Clinical Decision Suite can help sponsors enhance trial efficiency.

  9. Combining De-Identified EHR And Claims Data 5/8/2025

    Learn how EHR+ Data can improve your understanding of the patient's journey in ophthalmology, urology, and neurology clinical trials.

  10. Global Compliance Made Easy 5/6/2019

    Global clinical trial disclosure compliance is inherently complex, with over 39 registries, Most sponsors simply lack visibility into all the places they need to disclose information or what their commitments are. Automation can help make global compliance easier.