Trial Management STREAM

  1. Defining And Implementing The Right Oncology Digital Strategy 11/7/2024

    A panel of oncology experts shares how top life science companies are using a combination of DHTs, ePROs, clinical trial platforms, and more to ease oncology research and drastically reduce timelines.

  2. Learning About The Sensors In myMedidata 9/16/2025

    Learn how sensor data and advanced analytics can transform clinical research and enable your study to overcome data challenges, improving patient care.

  3. Cognitive, Pharmacodynamic Testing During FIH CNS Trials 5/22/2024

    A comprehensive review of optimal timing and methodologies for cognitive and pharmacodynamic testing during first-in-human trials on CNS-active compounds.

  4. Tailored Sponsor Engagement Key To Unlocking Site Network Efficiency 4/25/2025

    Karri Venn, VP site advocacy and mentorship at SCRS, emphasized the importance of sponsors recognizing the structure and capabilities of larger site networks.

  5. Perceptive eClinical 11/11/2024

    Learn about a randomization and trial supply management (RTSM) solution that helps keep your trial on track.

  6. End-To-End Clinical Data Flow 6/24/2024

    Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.

  7. Tackling The EU CTR Compliance Challenge 10/4/2018

    Maintaining disclosure compliance is tricky enough with ClinicalTrials.gov, but when it comes to EU CTR compliance, the complexity rises to a whole new level. As a sponsor, do you find your organization “guilty” of these common errors?

  8. Cohort Configuration Feature Of An RTSM Platform 3/16/2026

    Master trial agility by building and prioritizing cohorts in real time. Effortlessly manage dose levels and enrollment limits to keep your study on track, even as protocols evolve.

  9. Optimize Protocols For More Successful Trials 9/17/2024

    Find out how you can harness the power of AI and world-class data to recommend endpoints and inclusion/exclusion criteria for streamlined protocol design that results in more positive trial outcomes.

  10. Going From Good To Great As A TMF Champion 12/8/2023

    Gain insight into regulatory nuances, best practices for documentation management, and strategies for fostering a culture of compliance within the team.