Featured Articles

  1. 5 Key Takeaways From The FDA's Real-World Evidence Guidance 8/19/2024

    With our advanced technology and expertise, sponsors can confidently conduct RWE studies that are efficient and aligned with the FDA’s data-driven vision for healthcare.

  2. How Optina Diagnostics Used EDC In Earlier Disease Detection 5/15/2024

    Understand how Optina Diagnostics streamlined operations and achieved significant milestones by leveraging Castor's tools in its effort to revolutionize the diagnostic process for Alzheimer’s.

  3. Measuring The True Patient Experience 5/15/2024

    Utilizing the insights covered in this article can inform the design and implementation of cancer trials, ultimately contributing to improved patient care and treatment outcomes.

  4. ISR Report Sheds Light On eCOA/ePRO Market Dynamics 5/15/2024

    This comprehensive overview highlights the critical role these platforms play in modern clinical research, emphasizing their impact on data integrity and trial efficiency.

  5. eConsent Readiness In 24 Countries 3/12/2024

    Discover how regulatory bodies worldwide, including the U.S. Food and Drug Administration and the European Medicines Agency, are now championing the shift towards eConsent adoption.

  6. 10 FAQs On eConsent 11/16/2023

    Closely examine the challenges of adoption, integration, and compliance measures involving eConsent and gain valuable insights for those contemplating their incorporation in clinical trials.

  7. Essity Uses eConsent To Optimize Enrollment 8/15/2023

    See how a global hygiene and health company was able to deploy virtual methods through a strategic partnership to recruit and retain participants, streamline consent, and analyze patient data.

  8. How Electronic Source Data Revolutionizes Clinical Research 7/14/2023

    By increasing interoperability and embracing digital solutions, see how the research community can maximize the benefits offered by eSource, leading to improved trial outcomes and data quality.

  9. Preparing Studies With eConsent For IRB Approval 6/7/2023

    Understand how eConsent can benefit trials and align with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models.

  10. Unlocking The Power Of Real-World Evidence In FDA Submissions 5/15/2023

    Understand the gaps between how data is collected in real-world evidence (RWE) and randomized clinical trials (RCT) and how RWE is quickly finding ways to catch up.