eCOA Resources

  1. Introducing eCOA+ Streamlined Evidence Generation 1/16/2024

    Watch as Colin Weller, Vice President and General Manager of the Digital Outcomes and Evidence Platform at Medable, Inc., articulates the vision for eCOA+ and the trajectory of evidence generation.

  2. Letter From The CEO: A New Era Of Drug Development Is Here 9/3/2024

    This letter from Medable CEO Michelle Longmire lays out why we created Studio, what it enables sponsors and CROs to do, and how it will help everyone bring more effective therapies to patients faster.

  3. The Case For Cognitive Assessments In Phase 1 Clinical Trials 7/16/2024

    Regulators prioritize patient-reported outcomes. Cognitive assessments in Phase 1 trials detect early drug-related cognitive effects, ensuring safety and efficacy. Signant’s CDR System® is a proven tool for this.

  4. Shaping The Future Of eCOA User Acceptance Testing 9/24/2024

    Proactive planning by sponsors and early User Acceptance Testing (UAT) involvement in the eCOA design process can substantially improve study quality, efficiency, and consistency.

  5. eCOA Licensing Guide 3/7/2024

    In this comprehensive guide, IQVIA's eCOA library and licensing specialists, Kayla Doyle and Piero Bindi, explore five essential steps for obtaining licenses for the assessments required in your clinical trial.

  6. An Honest Assessment Of eCOAs From A Site Perspective 10/30/2023

    Listen to what sites have to say about the changing nature of COAs in clinical trials, including the usage of eCOA, its benefits, and ways to improve the technology.

  7. How SaaS Unlocks New Possibilities For Life Science Organizations 11/21/2024

    The rise of SaaS (software-as-a-service) has transformed industries, including life sciences, by enabling new possibilities. See how it’s already helping life science organizations around the world today.

  8. Taking Advantage Of EMA CTR For eCOA Studies In EU 7/13/2023

    Discover how sponsors can save time and effort by applying for clinical trial authorization once across the EU using the Clinical Trials Information System (CTIS).

  9. How Site And Patient Research Optimizes Clinical Trials 6/17/2024

    Signant’s patient and site research enhances digital health technology in clinical trials by optimizing usability and design. These insights drive improvements in product features, study designs, and training materials.

  10. The Real Cost In CNS Trials: Rater Drift And Site Readiness 11/21/2025

    Learn how to build resilience into CNS trial operations with evidence-based frameworks that prioritize human factors alongside digital tools.