Articles, App Notes, Case Studies, & White Papers

  1. Simple, Cost-Effective Ways To Engage Patients Using eCOA And IRT 9/7/2022

    Today, patients are exposed to sophisticated technology, which presents a huge opportunity to elevate engagement. Consider some common elements when initiating engagement during clinical development.

  2. Why Oncology Drug Development Lags In Digital Biomarkers 5/23/2023

    Despite technological advances, oncology drug development research has lagged in adopting wearable digital biomarkers. Explore this space's unique challenges and the benefits of wearable technology.

  3. Navigating The Next Wave Of Innovation In eCOA 7/30/2025

    Learn how the right eCOA system enables site efficiency and elevated data quality, ensuring trials run smoothly and deliver more reliable results.

  4. Do CROs Need To Reinvent Themselves In 2025? 3/21/2025

    Facing economic pressures, regulatory changes, and technological advancements, CROs must redefine their value propositions and discuss the need for reinvention in 2025 to accelerate into the future.

  5. Balancing Clinical Care With Digital Utility In Hybrid Trials 10/24/2022

    To create an effective decentralized clinical trial, tools and methods must be considered within the context of challenges faced by the clinical trial’s patients, physicians, and sites.

  6. 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.

  7. eCOA/ePRO: Why Patients Deserve Even More Progress 5/11/2022

    The shift from reporting on paper to reporting electronically has been happening for years, however, the transition hasn’t always been elegant. Explore how the pandemic has played a role in accelerating the shift to eCOA/ePRO.

  8. 5 Best Practices For Getting Started With ePRO 9/16/2024

    Unlock the potential of electronic Patient Reported Outcomes (ePRO) in your clinical research by implementing these essential best practices for success.

  9. Leading eSource Software Company Receives Part 11/Annex 11 Verification 9/26/2023

    Uncover how an independent confirmation of compliance opened up new opportunities and is instilling confidence in customers who are integrating the eSource system into their software validation strategy.

  10. RWD: More Than Just Another Acronym 10/19/2023

    Uncover how real-world data can not only be used for any type of clinical trial, but study sponsors can also use RWD to inform all stages of a study.