EDC, ePRO, eConsent

  1. Could ePRO Be The New Standard In Health Reimbursement? 1/30/2023

    Recently, early-phase protocols have been collecting patient-reported outcomes (PROs) not only to get regulatory approval but to demonstrate value to public and private payers.

  2. Gain The ePRO Advantage With Real-Time Data Collection 12/2/2022

    Discover how ePRO automatically incorporates eCOA data into a study, improving the depth, timeliness, and accuracy of patient-reported outcomes data in the following ways.

  3. 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.

  4. Start With 'Why' When Adopting New Tech To Support Hybrid Decentralized Trials 10/11/2022

    In this article, focus on the adoption of new clinical trial technology and explore how sponsors can support sites as they select and implement technologies.

  5. Better eConsent Through Education Best Practices 9/23/2022

    eConsent can have a positive impact on participant retention, but learn why that is only part of the challenge of meeting participant needs in a clinical trial.