On-Demand Webinars

  1. 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.

  2. Accelerate Parkinson's Drug Development With Active, Passive DHT Monitoring 4/15/2025

    Discover how a new ActiGraph–Indivi partnership is enhancing neurology clinical trials with digital health technologies that enable more sensitive, real-world outcome measures.

  3. Adopting Vault CDMS Accomplishments And Lessons Learned 8/31/2022

    GSK leveraged an agile approach and modern ways of working to help shorten their EDC build times. Learn how they reduced EDC build and UAT times by 50% and had all new studies built within Vault CDMS in 18 months.

  4. 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.

  5. Collect Better Oncology Trial Data, Easier 3/29/2022

    In this webinar, experts discuss how enriching oncology clinical trials with RWD generates deeper insights and improves operational efficiency to achieve better patient outcomes.

  6. Addressing Site And Sponsor Challenges In Digital Trials 10/10/2023

    <p>While the digital transformation of clinical trials has made tremendous strides in recent years, the plethora of new technologies can overwhelm. Learn how to help sites and sponsors combat the overload of technology.</p>

  7. RTSM Considerations For Master Protocol Oncology Studies 1/20/2022

    This webinar discusses the types of master protocols and how configurable, modern RTSM systems enable fast and seamless mid-study changes to help you efficiently run your master protocol study.

  8. Applying RWD: Use Cases And FDA Guidance 9/17/2024

    This presentation delves into pragmatic approaches for clinical evidence generation and regulatory acceptance. It examines recent FDA draft guidance on integrating RWD/RWE in medical device studies.

  9. Building One Home for Sites 7/23/2024

    Watch this presentation and demonstration of One Home for Sites for the latest updates on how the industry is coming together — even competitors — to alleviate the technology burden on research sites.

  10. Navigating Successful eConsent Adoption From Sponsor To Site 10/17/2023

    Drawing inspiration from real-world instances within the pharmaceutical and medical device sectors, watch as industry experts unravel the pivotal role of eConsent in optimizing modern clinical trials.