E-Technologies STREAM

  1. Preparing For 2022 1/19/2022

    2022 will be an important year for drug development. There are many questions around changes that came into play during the pandemic. A panel of experts look back over the year and into the future to help you prepare for the coming year.

  2. 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.

  3. 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.

  4. Overcoming TMF Management Challenges For Small And Mid-Sized Companies 2/10/2021

    Maintaining an inspection-ready Trial Master File is becoming increasingly burdensome, even for teams with significant resources. In this webinar our experts walk through a new, full-service TMF management approach implemented by smaller biopharmaceutical companies. By adopting a fixed-fee, turnkey model encompassing everything required for ongoing TMF health, these organizations are achieving high-quality TMF compliance – with far less effort.

  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. IQVIA eCOA Scribe Application 3/27/2025

    Experience seamless, secure, and flexible eCOA data collection with our application designed for diverse users, compatible with multiple devices, and equipped with offline functionality and robust authentication.

  7. Real-Time Data Tracking And Compliance Monitoring 3/27/2025

    Unlock real-time data tracking, customizable reporting, and proactive compliance monitoring with the IQVIA eCOA Sculptor Portal to enhance clinical decision-making and ensure protocol adherence.

  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. 2021 Predictions: Getting Down To Business In Clinical Trials 2/10/2021

    In this interactive webinar, a panel of clinical trial experts discusses observations from 2020 and suggests solutions and process improvements to help going forward. Topics range from site satisfaction and adoption best practices, decentralized trial technology, patient convenience and diversity.

  10. End-To-End Clinical Data Flow 6/24/2024

    Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.