Articles, App Notes, Case Studies, & White Papers

31. A Custom IRT System Facilitates Precision Medicine Studies 1/29/2025

    As the industry continues to embrace personalized medicine, the ability to implement and support an atypical supply chain is crucial.

32. Leveraging eCOA To Improve Patient Adherence In Clinical Trials 2/7/2025

    Patient adherence is one of the biggest challenges in clinical trials. eCOA solutions offer intuitive and engaging tools that encourage participants to complete their assessments on time.

33. Customizing EDC Workflows For Specialty Pharma, Rare Disease Trials 10/9/2025

    Rare disease and specialty pharma trials demand a level of flexibility with electronic data capture systems that can adapt dynamically without sacrificing data integrity.

34. Developing Drugs For Rare Diseases: Generating Clinical Evidence 5/13/2025

    For rare diseases, scientific breakthroughs often stall before reaching patients. A new approach to generating clinical evidence could change that trajectory.

35. With The Emergence Of DCTs, Do We Really Need A CTMS? 5/11/2023

    As decentralized trial designs continue to grow in popularity, do sponsors and CROs really need a clinical trial management system? Explore whether CTMS is necessary with the emergence of DCTs.

36. How Partnership Ensured A Successful First Digital Trial 5/1/2024

    Discover how this collaborative approach and tailored recommendations led to the successful implementation of an eConsent tool for a kidney cancer study with U.S. Renal Care.

37. Overcoming Oncology Trial Challenges With ePRO Solutions 5/16/2023

    Discover effective strategies and solutions to overcome challenges in oncology studies and how to optimize trial design, patient recruitment, data management, and regulatory compliance.

38. How To Overcome The Problem Of The Early ePRO Oversell 11/14/2022

    In this blog, explore how the approach to PROs needs to be reconsidered, given increasing regulations and trial scrutiny, the clinical need for patient-reported outcomes, and the ability to drive costs down and move off paper.

39. How Site eSource Completes And Extends The EHR To EDC Initiative 7/7/2025

    This study evaluates to what degree an eSource-to-EDC data transfer initiative succeeds through two key dimensions: "Mappability" and "Prevalence".

40. Digital Medicine Society Accelerates Recruitment and Results With eConsent 9/26/2022

    Find out how the Digital Medicine Society (DiMe), an interdisciplinary professional society for digital medicine, was able to deploy an eConsent module in less than two weeks to support its remote study to assess nocturnal scratching as an endpoint for patients.