Patient Data Reporting White Papers & Articles

  1. EHR-To-EDC: Choosing The Right Solution For Clinical Trials 12/13/2024

    Here we highlight key advantages of EHR-to-EDC eSource, such as cost-effectiveness and improved site satisfaction.

  2. Electronic Hauser Diary For Parkinson's Clinical Trials 12/9/2024

    In honor of World Movement Disorders Day, we highlight advances in Parkinson’s disease care. At the 2024 MDS Congress, Signant presented research on electronic diaries for tracking PD patients' functional status.

  3. Maximizing Site Performance: The Hidden Benefits Of Unified eConsent And EDC 12/6/2024

    Disconnected systems for eConsent and EDC create inefficiencies that burden clinical trial teams, but modern integrated platform solutions are streamlining operations.

  4. How Modern EDC Systems Are Becoming Clinical Intelligence Hubs 12/6/2024

    Modern electronic data capture (EDC) systems are transforming clinical trials by evolving from data repositories into dynamic clinical intelligence hubs.

  5. From Imaging To Analysis: 5 Steps For Success With TrialKit PACS 12/6/2024

    Obtain a fully integrated platform that seamlessly connects imaging data with EDC systems, resulting in streamlined data acquisition, real-time collaboration, and advanced analysis within a unified system.

  6. The Science Behind Medable's Health Economics And Outcomes Research 11/21/2024

    Meet the team responsible for ensuring the scientific rigor and outcomes of Medable’s clinical trial platform, and uncover how they’ve been pioneering eCOA and ePRO research for decades.

  7. eCOA Evolution: Have We Overcomplicated It? 11/21/2024

    eCOA has evolved from simple data collection to complex patient engagement platforms, raising concerns about added complexity. Explore innovative tools aimed at simplifying this complexity.

  8. Waiver Of Consent vs Waiver Of Written Consent 11/21/2024

    Learn the distinctions between a Waiver of Consent and a Waiver of Written Consent in clinical trials, and the importance of informed consent, particularly in the context of virtual trials.

  9. 7 Key Considerations For Designing The Optimal IRT/RTSM 11/21/2024

    Sponsors can create IRT/RTSM systems that are not only efficient and reliable but also adaptable to the evolving needs of clinical research by focusing on these seven key considerations.

  10. 3 Study Areas Where Your IRT Vendor Should Do More 11/21/2024

    Find out how advanced IRT systems now support diverse trial designs and how the expertise of RTSM vendors is crucial for tailoring solutions to trial needs and providing ongoing support.