Patient Data Reporting White Papers & Articles

31. Feasibility/Site Selection Process Ripe For Improvement 4/1/2025

    One key to a more effective feasibility process is more transparent communications and collaboration between sponsors, CROs, and sites. Sponsors must provide clear information to each site to enable a more accurate recruitment assessment, and sites must properly digest the information to give an accurate projection. But how?

32. Why Empowering Sites Matters 3/27/2025

    The evolving landscape of clinical trials demands a site-centric approach to address the increasing complexities of patient recruitment, study start-up, and data management.

33. The Catch-22 Of eConsent: A Missed Opportunity For Improved Trials 3/21/2025

    Drawing on evidence from scientific literature, we examine the pitfalls that have hindered its success and propose actionable solutions to unlock its true value in clinical research.

34. eTMFs Uncovered: 5 Costly Misconceptions To Avoid 3/21/2025

    Critically examine prevalent myths surrounding electronic Trial Master Files (eTMFs) and their integration with electronic Investigator Site Files (eISFs).

35. Strategies To Minimize Participant And Healthcare Provider Burden 3/21/2025

    Patient-reported outcomes (PROs) are vital for clinical trials but can burden participants and providers. Discover strategies and practical solutions to ease these burdens and improve data quality.

36. Driving Diversification And Reach With Tech In Community DCTs 3/20/2025

    Learn how technology, when used correctly, can accelerate trial timelines and drive patient diversification in community-based decentralized clinical trials (DCTs).

37. Achieving Best Outcomes With TMF Document Processing 3/18/2025

    TMF document processing requires a delicate balancing act. Sponsors strive for accuracy and completeness, but timeliness is crucial. How can teams achieve all three? Here are some practical strategies.

38. The Important Role Of The Study Owner In Guiding The TMF 3/18/2025

    Learn about the critical role that a study owner plays in maintaining Trial Master File (TMF) oversight, ensuring compliance, and driving collaboration across clinical study teams.

39. Safeguarding Personal Data: Protecting PII 3/17/2025

    Learn about a secure, patient-centric platform that enables individuals to participate in clinical trials and registries while maintaining lifelong access to their data.

40. The Role Of Technology In Transforming Dermatology Clinical Trials 3/17/2025

    AI and data-driven innovations are transforming dermatology clinical trials by enhancing efficiency, data accuracy, and patient access.