E-Technologies STREAM

  1. 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.

  2. Unleash The Power Of IQVIA Complete Consent 11/12/2024

    Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.

  3. An AI Action Plan For The TMF Professional 6/12/2024

    Explore AI's impact on TMF processes in this on-demand webinar. Gain clarity on AI's potential, key evaluation criteria, and practical applications for enhancing TMF health and inspection-readiness.

  4. 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.

  5. Successful Subject Creation With eCOA, eConsent, & IRT Process Flow 5/26/2023

    Watch a short walkthrough of how IRT and electronic Clinical Outcome Assessment (eCOA) solution on a unified platform delivery drives smoother study orchestration.

  6. Medable Total Consent: The Future Of Informed Consent 2/14/2023

    With Total Consent, Medable is transforming the consenting process – harmonizing it into one simple-to-use platform that enables trial sponsors and CROs to completely customize eConsent.

  7. Right-Size Your eConsent Approach 11/17/2023

    Delve into the art of tailoring the eConsent experience to match your study and patients' specific needs, such as crafting eConsent documents, selecting appropriate delivery models, and more.

  8. Selecting And Expanding Your EDC System: A Testimonial From Everest Clinical Research 4/25/2025

    Everest Clinical Research shares what lead them to strengthen their partnership with Medidata, and expand past the use of Medidata's EDC products too other helpful solutions.

  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. Fast, Flexible, And Proven Direct-From-Patient Data Capture With eCOA 5/3/2022

    Delve into how IQVIA eCOA captures patient data in a way that always keeps patients top of mind.