ePRO Resources

  1. Pharmaceutical Company Gets Unified Decentralized Platform 2/28/2023

    Unearth how this global eClinical provider delivered a decentralized platform including eSource/ePRO for direct-data-entry, randomization, eConsent, telehealth, remote monitoring, and data management.

  2. Simplify Today. Transform For The Future. 10/25/2023

    Maximize efficiency today with a cloud-based user-friendly platform that seamlessly adapts to the future of phase 1-3 trials. Watch to see how Zelta can help.

  3. Still Using Paper Diaries To Capture PRO Data? Read This. 1/8/2024

    Access real-world examples of how electronic patient-reported outcome measures (PROMs) optimize data quality and reliability and improve the statistical power of trial data.

  4. What Universalized Terminology Means For Decentralized Research 10/26/2022

    Many DCT stakeholders have attempted to release terminology guides as it relates to their own dealings, however, there had never been a wide range of universalized DCT terms until now. 

  5. Site Perspectives On BYOD ePRO Use 6/17/2024

    This study examines participant convenience and compliance, aiming to understand and address the challenges faced by site personnel in global trials.

  6. Headed Down Registry Road? Here Are The EDC Features You'll Need 3/18/2022

    Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.

  7. 5 Best Practices For Getting Started With ePRO 9/16/2024

    Unlock the potential of electronic Patient Reported Outcomes (ePRO) in your clinical research by implementing these essential best practices for success.

  8. How To Overcome The Problem Of The Early ePRO Oversell 11/14/2022

    In this blog, explore how the approach to PROs needs to be reconsidered, given increasing regulations and trial scrutiny, the clinical need for patient-reported outcomes, and the ability to drive costs down and move off paper.

  9. Solutions For Sponsors Utilizing Drafted Guidance For PROs In Oncology 11/20/2024

    Explore the challenges pharmaceutical companies face in implementing PROs in cancer clinical trials as outlined in the FDA’s draft guidance, as well as strategies to overcome these obstacles.

  10. The Benefits Of Real-Time ePRO/eCOA In Clinical Trials 10/4/2024

    TrialKit addresses data management issues in clinical trials through its innovative ePRO and eCOA tools, which facilitate real-time data collection and reporting.