On-Demand Webinars

  1. Accelerating DHT Research And Drug Development 12/19/2024

    This presentation focuses on the scope and utility of the National Health and Nutrition Examination Survey, a program of studies designed to assess the health status of individuals in the United States.

  2. How FAIR Data Principles Power Clinical Analytics Success 11/8/2023

    Explore key challenges in accessing and preparing analytics-ready clinical data, how FAIR guiding principles can help maximize the value of clinical trial data, and the impact of innovative analytics.

  3. The Revival Of Electronic Informed Consent 11/2/2022

    The clinical research industry has been reluctant to adopt eConsent for several reasons. Unearth how the industry should continue exploring and implementing digital technologies in earnest in the future.

  4. How Recent Regulations Are Helping Advance eCOA And ePRO 8/17/2023

    Consider new perspectives on 2023-issued guidance by the EMA and FDA, and how the amalgamation of these directives, combined with scientific insights, can empower sponsors and biotech firms.

  5. An Introduction To One Home for Sites™ 4/18/2024

    This on-demand webinar provides a thorough overview of why IQVIA Technologies is building One Home for Sites, how it works, and who should participate.

  6. eConsent – The Enrollment Solution For Decentralized Trials 2/1/2022

    The COVID-19 pandemic and the increased technological competence required to enroll and retain research participants has left many organizations wondering how to modernize their enrollment and consent process. Find out more about the landscape and its impact in the available webinar.

  7. Practical Approaches To Faster Study Start-Ups 9/25/2023

    Learn how teams can leverage organizational, procedural, and technological solutions to recapture valuable days, weeks, and even months in the activation timelines of research sites.

  8. FDA's Vision On PRO Collection For RWE 9/24/2024

    In this presentation, a distinguished panel of experts illuminates the crucial role of patient-reported outcomes (PROs) in shaping regulatory decisions and drug development strategies.

  9. Are You Ready For Fully Remote eCOA In Your Next DCT Trial? 12/16/2022

    Watch to learn how you can build a better data management and compliance monitoring plan for your COAs in your next DCT trial.

  10. Top 10 Questions For Selecting The Best eTMF System 4/11/2022

    An eTMF system can help Clinical Operations professionals manage the deluge of documents and data, but what capabilities are right for your situation? What is the best way to make the move to a modern eTMF from paper, spreadsheet trackers, or legacy tech to a new eTMF? Hear answers to these questions and more from a fellow Clinical Operations leader with experience in making the transition to an eTMF built for today's research ecosystems.