Articles, App Notes, Case Studies, & White Papers

31. RBQM For Decentralized Trials: Two Key Areas Of Focus To Reduce Your Risk 9/26/2022

    This article takes a more in-depth look at Sections 5.0.5: ‘Risk Communication’ and 5.0.6: ‘Risk Review.’ in ICH-GCP E6 R2 to show how the implementation of RBQM can reduce issues and achieve holistic trial oversight in today’s complex decentralized trials.

32. Affordable Clinical Trial Data Management Without Compromise 6/4/2024

    Discover how TrialKit can revolutionize your approach to clinical research data management, making it efficient, scalable, and affordable without compromising quality or functionality.

33. Precision Recruitment: Fixing The Future Of Clinical Trials 10/21/2025

    Explore how to design ethical, effective, and patient-centric AI-powered recruitment pipelines that truly connect the right patients to the right trials.

34. Unlocking The Value Of AI In IRT: Practical Perspectives From Vendors 12/5/2025

    AI can enhance IRT with predictive modeling and automation, but true success relies on high-quality data, compliance, and user trust. Learn practical strategies to boost efficiency.

35. Expanding Flexibility Of eCOA Data Collection With Controlled Interview Mode 1/31/2022

    Discover how the interview mode constitutes an additional data entry mode for ePROs when clinical trial participants cannot go to the study site for a scheduled visit.

36. The Future Of Remote Patient Monitoring In Decentralized Clinical Trials 5/8/2025

    Remote Patient Monitoring (RPM) is not just an innovation—it's a catalyst redefining how clinical research is conducted in the digital age.

37. A Checklist For Good TMF Health 10/16/2023

    The Trial Master File serves as the central repository of documentation. Utilize this guide to better concentrate on critical considerations and safeguard the well-being of your TMF.

38. Putting Trial Data Insights Into Action For Your Study 10/21/2025

    Learn why sponsors should implement an integrated data monitoring plan and technology solution to ensure data integrity, meet evolving regulatory requirements, and improve trial outcomes.

39. Atlantic Research Group Builds Competitive Advantage With Medrio EDC 1/30/2023

    By using Medrio’s EDC platform, learn how Atlantic Research Group was able to achieve the flexibility needed to span multiple therapeutic areas and eliminate redundancy in documentation.

40. 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.