Trial Management STREAM

  1. TMF Management In Clinical Trials 3/13/2023

    Elevate your knowledge of clinical trials and the Trial Master File by exploring three critical topics.

  2. Think U.S.A.: The Operations Behind Your Clinical Trials 1/22/2025

    Ready to think differently about early-phase clinical development? Check out the spotlight on our U.S. clinical facilities and the incredible teams behind them.

  3. Are Your Clinical Study Meetings Building Momentum, Or Wasting Time? 9/17/2025

    Transforming passive clinical trial meetings into active catalysts for success, aligning teams and accelerating timelines.

  4. Clinical Research Without Borders 5/16/2024

    Explore strategies for navigating global clinical trials with, Afshawn Chakamian of Avidity Biosciences, Dr. Amy Raymond of Worldwide Clinical Trials, Scott Schliebner of Novotech, and Scout’s KimberLee Heidmann.

  5. Patient First Solutions For Oncology 2/14/2023

    Medable, Inc's new oncology offering is an end-to-end suite that includes an extensive eCOA library, pre-built and validated DCT applications such as Total Consent and Televisit, and protocol design consulting.

  6. 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.

  7. Build Your Diversity Action Plan With AI And Patient Insights 5/29/2024

    Discover how AI and patient insights can help you build a compliant Diversity Action Plan and overcome barriers to achieve diverse clinical trial enrollment.

  8. Webinar: Reimbursement Methods For Sustainable CGT Business Models 10/10/2023

    Learn more about the key features of successful innovative pricing and reimbursement models as well as outcomes-based agreements and the ways to advance those strategies for cell and gene therapies.

  9. 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?

  10. Investigator SmartSelect 10/23/2024

    This advanced recommendation engine identifies protocol-specific investigators in just minutes, dramatically shortening a process that typically takes four to six weeks.