Articles, App Notes, Case Studies, & White Papers

31. Enhancing Participant Payments: A New Approach 10/30/2024

    Managing participant payments in clinical trials is a multifaceted challenge impacting participants, sites, and sponsors alike. Delve into the intricacies and numerous hurdles faced in this process.

32. 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.

33. Guide: Switching To A New EDC System 6/24/2024

    Read to learn five key tips when switching to a new EDC system, including best practices for change management, process and people training, KPIs, and more.

34. Data Integrity In Clinical Trials: The Role Of Advanced EDC Systems 10/7/2024

    How can Electronic Data Capture (EDC) tools streamline your data collection process and help you manage the increasing complexity and data?

35. 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.

36. Digital Measurement Of Nocturnal Scratch In Atopic Dermatitis 5/9/2025

    A major challenge in managing atopic dermatitis (AD) is the lack of objective tools to measure the impact of nocturnal scratching, but new digital measurement solutions could address this gap.

37. Driving Enrollment Predictability In Clinical Trial Timelines 1/13/2025

    Missed enrollment targets cost millions—TA Scan’s benchmarking and simulation tools empower sponsors to forecast with confidence, optimize site strategy, and keep budgets on track.

38. Reduce Time, Cost, & Risk With Clinical Study Data Review Software 1/22/2021

    See how a top 10 global biopharmaceutical company implemented a single data review system to reduce the time, cost, and risk of running its clinical trials while accelerating the time to market.

39. 3 Proven eConsent Implementation And Adoption Best Practices 1/19/2024

    By advocating these three essential best practices, learn how stakeholders can navigate the complexities of eConsent adoption with confidence and enhance the overall efficiency and success of clinical trials.

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.