Data Management STREAM

  1. Manage Exponential Data Growth With Medidata Clinical Data Studio 6/19/2025

    Bring study teams together like never before for total data quality oversight.

  2. 2 Of The Most Impressive AI Applications 1/27/2025

    Elena Sinclair reveals the only two (out of 12) applications of AI in clinical development that McKinsey identified as decreasing costs, improving timelines, and increasing probability of success.

  3. Improving Supply Chain: Accountability, Sustainability, Optimization

    Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.

  4. The Role Of Technology In Improving Site Performance 5/29/2025

    Explore how clinical trial sponsors can benefit from the growing use of electronic source (eSource) technology at research sites.

  5. Introduction To An End-To-End Clinical Data Science Platform 3/25/2024

    Watch to learn about an end-to-end clinical data science platform designed to streamline the rapid generation of deep insights from clinical trial data, enabling efficient delivery of crucial analyses.

  6. TMF Migrations: Streamlining The Journey To An Inspection-Ready Result 9/18/2023

    Delve into several techniques designed to safeguard data precision and integrity throughout the TMF migration process, reducing compliance risks and conserving valuable time and effort.

  7. 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.

  8. Patient-Level Clinical Trial Data + Real World Data 9/6/2022

    Future-proof your clinical trial and enhance your evidence generation activities with Medidata Link, which allows sponsors to collect clinical trial data and link it at the patient level to real-world data (RWD).

  9. The FDA's View Of AI In Clinical Trials Is Limited 1/27/2025

    Tala Fakhouri explains that there could be so many more applications of AI in clinical development than what the FDA sees in regulatory submissions.

  10. 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.