On-Demand Webinars

  1. Securing High-Quality Patient Referrals From HCPs...Faster! 10/13/2023

    Looking to minimize time on outreach or accelerate patient recruitment? Uncover how this partnership was able to deliver positive overall results for sponsors, ultimately benefiting patients.

  2. Clinical Trial Management System 4/22/2022

    Watch to learn the reasons why research sites, site networks, health systems, academic medical centers, and cancer centers use a CTMS to centralize information related to protocols, subjects, staff, financials and billing, and much more.

  3. Leveraging Internal And External Insights For Precision Enrollment Modeling 1/28/2025

    Discover a trial feasibility tool that integrates users' operational insights with high-quality clinical intelligence to drive accurate and informed enrollment projections and site capacity analyses.

  4. Accelerating Rare Disease Drug Development With Wearable DHTs 12/8/2023

    Watch as experts from ActiGraph, Bellerophon Therapeutics, and IQVIA come together to explore the obstacles and potential breakthroughs in rare disease research.

  5. Exploring The Role Of Wearable Biosensors Within The DCT Ecosystem 3/28/2022

    In this pre-recorded webinar, experts from the industry share real-world insights and practical guidance on how to achieve success in decentralized clinical trials.

  6. 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.

  7. Proven Practices For ePRO Adoption 12/8/2022

    Industry experts discuss how a medical device company implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.

  8. Big Roadblocks To Avoid When Implementing A New CTMS 6/9/2023

    Watch as presenters from Medidata dive into the most common roadblocks customers face when adopting a modern CTMS—and how to avoid them.

  9. Designing ePRO and eConsent Solutions that Participants and Sites Want 10/26/2022

    Participant-focused eClinical technologies offer significant potential to decrease paper-based processes and improve end-user experiences in collecting patient-reported outcomes (PRO) and informed consent, but many users continue to experience rigid technology, complicated hardware provisioning processes, and clunky implementations that leave sponsors, CROs and sites questioning the value. 

  10. PMCF Requirements: Questions On Cost, Device Viability, And Where AI Fits In 8/20/2026

    PMCF costs are straining device budgets. Discover how AI-assisted review and real-world data from other regions can help you meet EU requirements more efficiently.