On-Demand Webinars

1. Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations 2/22/2023

   Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.

2. Using Remote Image Capture eCOA For Hybrid Dermatology Trials 2/1/2022

   From eRecruitment, pre-screening, eConsent, and image-based data capture, explore how a decentralized trial design helps streamline enrollment, increase patient retention, and ensure data quality.

3. Transforming Oncology Trials With Next-Gen eCOA 6/9/2025

   With the FDA stating last fall that the “patient’s voice” is key to understanding real-world-impacts, eCOAs and ePROs are becoming quintessential tools for cancer trials.

4. Real-World DHT Adherence Insights And Good Practices 7/10/2025

   While advances in sensors and device design are improving wearability, successful data collection still hinges on participant adherence. The session highlights why addressing this can’t be an afterthought.

5. Amplifying Evidence With Unified Clinical Trial Data Collection 5/3/2024

   In this presentation, we explore the transformative potential of integrating a unified clinical trial data collection platform with intelligent automation, challenging the inadequacies of the status quo.

6. How ICH Oversight And AI Are Shaping The Future Of Clinical Trials 10/9/2025

   Explore how the new ICH E6 (R3) revisions are reshaping clinical trial oversight and examine how AI-driven tools like the Clinical Decision Suite can help sponsors enhance trial efficiency.

7. Right-Size Your eConsent Approach 11/17/2023

   Delve into the art of tailoring the eConsent experience to match your study and patients' specific needs, such as crafting eConsent documents, selecting appropriate delivery models, and more.

8. Advancing Heart Failure Research With Digital Measures 9/6/2023

   Digital health technologies can unlock meaningful insights. Explore the synergy between this cutting-edge technology and managing heart failure, and how it's paving the way for better patient care.

9. The Rise Of The Site: Empowering Efficient Clinical Study Execution 2/18/2025

   Join the Co-CEO of CRIO, as he explores research site challenges and how site-based technologies can reduce administrative burdens, enhance efficiency, and eliminate redundant one-time-use technologies.

10. 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.