On-Demand Webinars

  1. Reduce TMF Misfiles & Metadata Errors With Next-Gen AI-Enabled eTMF 4/17/2023

    Listen in as Chief Product Officer Jim Nichols, Product Manager Jim Horstmann, and VP Solutions Consulting Aaron Grant discuss issues and solutions for trial master files.

  2. From Paper To ePRO: Providing Flexibility And Efficiency 3/12/2024

    Explore the transformative impact of flexible ePRO technology on clinical trials, elucidating how it enhances patient-centricity and operational efficiency for sponsors.

  3. 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.

  4. Rethinking Effectiveness: Balancing Tradeoffs In An Era Of Disruption 11/12/2025

    In an era defined by rapid disruption and technological advancement, clinical operations leaders are under increasing pressure to enhance effectiveness while managing complex strategic trade-offs.

  5. The Top 5 Myths About eCOAs In 2025 5/15/2025

    Join leading clinical experts as they debunk the top 5 myths about eCOA in 2025, separating fact from fiction to help clinical operations, procurement, and data management teams make smarter decisions.

  6. No Code Requirement: Pre-Trial Insights For Operational Success 5/14/2024

    Discover how a no-code solution transforms insight generation from weeks to minutes. Learn to run analyses, test hypotheses, and enhance patient trial recruitment and diversity with ease.

  7. 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. 

  8. 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.

  9. 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.

  10. A Framework For Selecting Reliable Clinical Endpoints From Real-World DHT Data 2/25/2025

    Dr. Andy Liu presents a case study determining which digital measure of physical activity would be a well-defined and reliable clinical endpoint in a trial including patients with diabetes.