Articles, App Notes, Case Studies, & White Papers

  1. Building A Gold Standard Trial Experience In Japan 4/4/2025

    Hear how Medable worked with a Japanese sponsor to elevate their trial experience, achieve >90% patient and site adherence, and beat their forecasted FPI date, creating new eCOA standards adopted across all the customer’s vendors.

  2. Build Vs. Buy Vs. Partner In Life Sciences: Making The Right Call 3/21/2025

    Discover when life sciences organizations should develop technology in-house, buy off-the-shelf solutions, or form strategic partnerships, exploring the costs and risks that come with each approach.

  3. What Is The Suvoda Platform? 7/31/2025

    If you're ready to streamline your clinical trials and deliver better outcomes for all stakeholders, explore how the Suvoda Platform can transform your trial experience today.

  4. eSource vs. EDC: Reimagining Your Clinical Trials 5/29/2025

    Explore how an eSource approach to clinical trial data can reduce site burden, eliminate double data entry, minimize queries, and enhance remote monitoring.

  5. Benefits Of Delegating Your Oncology Trials Patient Screening Process 10/16/2024

    Explore the integration of Electronic Health Records (EHR) into oncology clinical trials, highlighting both challenges and potential advancements.

  6. Empowering Freenome: Large-Scale Data Quality And Compliance 10/17/2023

    Delve into five ways this biotech company was able to successfully deliver data quality and compliance for large-scale trials while developing next-generation blood tests for early cancer detection.

  7. Securing Sponsor Reimbursement For CRIO Fees 12/11/2025

    Gain sponsor approval by positioning technology as key to streamlined workflows, compliance, and patient safety — reducing risk and improving collaboration. Explore strategies now.

  8. eCOA Solution Design Recommendations: Applied Insights From Trial Sites, CRAs 6/17/2024

    Enhance hybrid trials with digitalization through remote data capture using smartphones, tablets, and computers, improving participant experience and data integrity.

  9. Understanding Various Site Use Cases For eSource And EDC 9/20/2023

    Learn how leveraging electronic data capture solutions can be pivotal in ensuring the successful execution of clinical research trials through expedited data processes, minimal errors, and more.

  10. Real-World Evidence - Where Are We Now? 8/24/2022

    Notwithstanding ongoing confusion over the concepts of “real-world data” and “real-world evidence” in 2022, more than 5 years after the passage of the 21st Century Cures Act, the FDA continues to evaluate such data and evidence as it considers regulatory decisions.