Patient Data Reporting Applications & Studies

  1. Real-Time, Remote Data Collection For Faster Trial Deployment 7/20/2022

    A leading pharma company was planning a Phase III trial for a SARS-CoV-2 prophylactic therapy and needed to evaluate post-exposure prophylaxis and preemptive treatment in 1,000+ patients at 82 sites. Explore how eSource was rapidly deployed for clinical trial success.

  2. Large NCI-Designated Hospital System Trains 400 End Users, Resulting In Increased Levels Of Efficiency And Consistency 6/28/2022

    Learn how an eLearning solution was used to help overburdened trainers from a large National Cancer Institute (NCI)-designated hospital system.

  3. Vanderbilt's Advice For Sponsors: How To Make Working With Your EDC Easier For Sites 5/24/2022

    Learn how research sites like Vanderbilt University Medical Center speed study timelines and drive higher quality data entry with a modern EDC.

  4. Top 10 Biopharma Achieves Significant Regulatory Efficiency 5/23/2022

    Discover how a top 10 biopharmaceutical company expanded its regulatory efficiency and automated key workflows between their IRB Platform and their electronic master file (eTMF).

  5. A Leading Academic Medical Center Monitors Newly Diagnosed Myeloma Patients 5/20/2022

    Learn how eCOA helped to motivate patients and increased engagement around experiences outside of the clinical setting, which otherwise may have gone unmentioned.

  6. Reata Saves Millions Leveraging The Adaptive Functionality Of RTSM 3/25/2022

    Embarking on a new cardiovascular Phase-II clinical study, Reata was challenged with finding a randomization and trial supply management (RTSM) solution that would accommodate the study’s highly adaptive trial design and detailed protocol. Uncover the solution in this case study.

  7. Long-Term Patient Engagement: Interoperability Micropayments Case Study 3/17/2022

    Delve into the details of this collaborative partnership and the strategies they used to boost engagement and eCOA compliance and garner positive participant feedback while alleviating site burden.

  8. Implantable Medical Device 11/29/2021

    A leading global medical device company received a warning letter from the United States Food and Drug Administration (FDA), citing a failure to comply with post-approval ePRO (electronic patient-reported outcome assessments) requirements related to a cleared implantable medical device. Find out what happens in the available case study.

  9. The Impact Of Mobile App Technology On eCOA 10/27/2021

    Patients are vital to the success of any clinical trial. Yet many trials struggle to keep patients engaged for the duration of the study.

  10. Achieving 97% Patient Compliance, Increased Patient Engagement 9/23/2021

    In a proof-of-concept for a decentralized hybrid study, explore how Electronic Patient-Reported Outcomes (ePRO) technology was used to assess the results of varying digital therapies and the feasibility of conducting a largely virtual clinical study in a fibromyalgia population.