E-Technologies STREAM

  1. Crossing The TMF Compliance Gap With Inspection-Ready Access For Closed Studies 4/30/2021

    Your drug study is closed, you need inspection-ready access to the Trial Master File, but your CRO is ready to get the TMF out of their system and wants to send you a zip folder full of documents. What do you do? In this session, we explore an innovative new way to ensure your TMF stays secure while remaining accessible to audits and inspectors so you can focus on getting your drug to market and not on finding documents. 

  2. Secrets To A Collaborative Model To Improve TMF Management 10/30/2023

    Speakers from Phlexglobal and Regeneron share the benefits of their highly effective partnering model and lessons learned that you can apply in your organization.

  3. Mastering Scientific Communication Plans Within Medical Affairs 2/6/2025

    Join industry leaders from Anju and 9 Labs for a presentation on the pivotal role of Strategic Communication Plans (SCP) in medical affairs.

  4. Get Your TMF Health Score 5/11/2022

    Introducing the TMF Health Score – an expert methodology that provides an “early warning system” to commonly overlooked issues that often lead to inspection findings.

  5. Closing The "Compliance Gap" In TMF Archiving 8/15/2022

    Discover how organizations are crossing this “compliance gap” with PhlexTMF for Viewing, an easily accessible TMF archive for internal use, audits, and inspections.

  6. An Honest Assessment Of eCOAs From A Site Perspective 10/30/2023

    Listen to what sites have to say about the changing nature of COAs in clinical trials, including the usage of eCOA, its benefits, and ways to improve the technology.

  7. IQVIA IRT - Putting The Focus On Driving Value For Our Customers 2/27/2025

    IQVIA IRT senior leader and expert, Dan Pavitt, highlights key IRT initiatives aimed at enhancing customer value in this Clinical Leader Solutions Expo presentation.

  8. BYOD Is Here To Stay 5/3/2022

    In this webinar, eCOA experts will explore how to implement a BYOD strategy, relevant BYOD regulatory considerations, and where the market is going from here.

  9. Harnessing The Potential Of Patient-Level Data In Clinical Trials   6/19/2024

    Join our panel of industry leaders as they explore innovative methods and best practices for incorporating fully consented patient data in clinical trials.

  10. Industry-First eTMF AI: PhlexTMF v21 4/6/2023

    Pre-trained on millions of documents and embedding the cumulative guidance of Phlexglobal’s TMF experts, uncover how teams can ensure clinical documents are “right-first-time” at document upload.