Data Management STREAM

  1. Collect Better Oncology Trial Data, Easier 3/29/2022

    In this webinar, experts discuss how enriching oncology clinical trials with RWD generates deeper insights and improves operational efficiency to achieve better patient outcomes.

  2. Improving The Quality Of Submitted Studies To ClinicalTrials.gov 11/7/2019

    Want to reduce QC comments? Hear tips from Dr. Deborah Zarin, former director of ClinicalTrials.gov, now with the MRCT Center. Dr. Zarin was keynote speaker at the recent EXTRA: TrialScope Transparency Experience.

  3. 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.

  4. Pharmaprojects By Citeline 1/19/2023

    With Pharmaprojects, leverage your mastery of the R&D space to create winning strategies, identify the right drugs to license, and support the key decisions that will drive your company forward.

  5. Streamline EDC Data Entry Using EHR Data 1/17/2023

    Explore how a clinical research coordinator (CRC) typically manually re-enters data from their EHR/EMR system into Rave EDC, and how Rave Companion provides automated assistance to enable the CRC to complete EDC forms.

  6. Keeping Your Trials In Motion And Use AI Where It Makes Sense 2/2/2026

    Explore the "pinball" approach used by the Judi platform that is giving stakeholders a distinct competitive advantage in the clinical trial landscape.

  7. TRACON: Reducing Clinical Trial Cost By Connecting Systems 8/14/2024

    Companies are gaining operational efficiencies with a single platform across R&D including CTMS, EDC, and Safety. Hear how one biotech is breaking down system silos and eliminating data reconciliation, reducing clinical trial costs by 70%.

  8. Citeline Study Feasibility 11/30/2021

    This predictive analytic solution helps sponsors select global study sites to successfully enroll more patients and accelerate clinical trial cycle times. Study Feasibility leverages both human expertise and machine-learning algorithms trained on Citeline’s best-in-class data.

  9. Streamline The Clinical Trial Disclosure Process 7/29/2024

    Core Data simplifies the registry submission and approval process by consolidating data for multiple registries into one single form, promoting consistency across registries and saving time by minimizing data entry.

  10. Yes, Your Study Is At Risk: Risk Mitigation Plans For Endpoints 1/15/2026

    Ocular endpoints often introduce unique bottlenecks that can stall enrollment and compromise data integrity. This presentation provides the tools for a streamlined, resilient clinical trial strategy.