Data Management STREAM

  1. 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.

  2. Amplifying Evidence With Unified Clinical Trial Data Collection 5/3/2024

    In this presentation, we explore the transformative potential of integrating a unified clinical trial data collection platform with intelligent automation, challenging the inadequacies of the status quo.

  3. 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. 

  4. The Many Facets Of Early Phase Evaluation Of Psychedelics In Psychiatry 2/3/2023

    Altasciences and Sygnature Discovery discuss the clinical and non-clinical studies required for evaluation of abuse risks of psychedelic drugs.

  5. Translating R3 Data Governance And Oversight Into Practice 7/18/2026

    Learn how to translate ICH E6(R3) into practice with actionable strategies for proactive risk management, robust data governance, and earlier deviation detection.

  6. Sitetrove: Industry-Leading Global Investigator And Site Intelligence 1/20/2022

    With over 500,000 investigators and more than 180,000 clinical trial sites spanning 185 countries, Sitetrove provides the data vital to accurately assessing target locations, identifying qualified investigators, and prioritizing candidates for clinical trial success.

  7. Case Study: Optimizing Clinical Supply Chain With Advanced Technology 4/24/2024

    In this interactive discussion, IQVIA Technologies'  IRT experts delve into real-world examples and practical AI applications.

  8. Medidata Research Alliance 2/21/2024

    The Medidata Research Alliance collaborates with scientific and medical research communities to use clinical trial data for medical advancements and increased patient access to innovative treatments.

  9. 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.

  10. Challenges To Making Go/No-Go Decisions In Clinical Trials 7/16/2026

    In drug development, a go/no-go decision can be a high-stakes trade-off between speed and certainty. Delve into the real-world operational and strategic hurdles to making those decisions.