On-Demand Webinars

  1. 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.

  2. Maximize Control And Transparency On The Path To Study Go-Live 10/10/2024

    Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.

  3. Optimizing Efficiency And Quality In EDC Implementation 3/21/2023

    Grant Williamson and Siba Noolu discuss best practices for ensuring quality and speed across EDC platforms for clinical operations, data management, and programming professionals.

  4. Oncology Research And Care: Reimagining Digital Innovation 8/25/2021

    During this webinar, speakers will discuss how they are successfully deploying wearable and remote monitoring technologies to improve clinical outcomes in patients living with cancer.

  5. Unleash The Power Of IQVIA eCOA: A Deep Dive 9/10/2024

    Edward Bartels, an expert in eCOA solutions, provides an in-depth overview of the market trends, emerging technologies, and how IQVIA eCOA is pioneering advancements in this space.

  6. 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.

  7. The Value Of Continuous Cough Monitoring And Its Impact On The Placebo Effect 5/9/2025

    This presentation explores how digital health technologies are transforming the way persistent cough is monitored and understood across various respiratory diseases.

  8. 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. 

  9. CTMS & Study Data: 2 Keys To Creating Optimal Process Transparency 5/8/2023

    Clinical trial management systems can either make or break operational workflows in medical studies. Listen to this discussion with Hope Weisser, Sr. Product Manager at TransPerfect, about the new features of Trial Interactive’s CTMS.

  10. Tailoring IRT/RTSM Solutions To Overcome Challenges 12/12/2024

    Learn how RTSM can be tailored to meet precision medicine’s unique challenges of expiry, visit & personalized shipment management.