E-Technologies STREAM

  1. 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.

  2. TMF Completeness: Simple Solutions For A Complex Problem 9/7/2021

    In this session, two of the top technology minds in TMF management will demonstrate and a simple yet innovative way to measure completeness at any point during the trial. 

  3. Deploy eConsent Around The World With Confidence 8/16/2022

    Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.

  4. Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials 6/24/2024

    Willie Muehlhausen, Co-CEO and Founder of Safira Clinical Research, and Tim Davis, VP of Strategy at MyVeeva for Patients, discuss how ePRO delivery needs to change to better serve modern trials.

  5. 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.

  6. 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.

  7. Selecting Medidata Rave: A Testimonial From Richmond Pharmacology 4/25/2025

    What made the Medidata's Rave EDC system stand out to Richmond Pharmacology during their vendor selection period?

  8. Digital Versus Digitized: Common Misconceptions About eConsent 7/27/2022

    In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.

  9. Enhancing Oncology Clinical Trials Through The Use Of Digital Technologies 3/30/2023

    The most difficult clinical research just became more challenging. Learn tactics on how teams can simplify oncology research while solving new and old issues.

  10. Taking A Risk-Based Approach To An Inspection-Ready Audit Trail 2/10/2021

    Regulatory agencies agree that a risk-based approach is the best way to ensure quality in clinical trials. But knowing how to implement such a process can be daunting. In this session, we will explore how to implement RBM to ensure your TMF Audit Trail is ready for inspection.