ePRO Resources

1. Rare Disease Clinical Trials: Modern Design And Supply Chain 10/12/2023

   Gain insight from several contributing experts for overcoming unique obstacles in rare disease research and learn how to better develop strategies.

2. Addressing The Specific Complexities Of Oncology eCOA Clinical Trials 4/18/2022

   What are the specific tools and keys to conduct eCOA trials in oncology successfully? This article identifies some of the relevant solutions to tackle oncology protocol complexities.

3. Why Capturing Pro Data Matters In Early-Phase Oncology Trials 9/26/2024

   If you are in the early stages of an oncology trial, there is a lot to consider when it comes to your data management and how the process can be simplified by improving how your study captures data.

4. Driving Customer Profitability With Enterprise Platform, Pricing 2/29/2024

   Explore how the solutions and approaches offered by CDS can help different research stakeholders conduct more cost-efficient clinical trials in the industry's pharmaceutical, biotech, and device sectors.

5. 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.

6. Why eConsent Makes Such A Difference In Patient Adherence And Engagement 6/6/2022

   Explore how consent is a critical step that can greatly influence patient enrollment, adherence and retention in the trial.

7. Interview Mode: A Valuable Data Collection Alternative Supporting DCTs 3/8/2022

   Download the available infographic to discover how collecting ePRO & eObsRO data via interview mode can be recommended in specific circumstances.

8. Medrio eCOA/ePRO 3/18/2024

   Take your ePRO clinical outcome assessments from clunky to convenient. Intuitive, configurable solutions improve the participant experience, site processes, and data quality, from protocol to postmarket.

9. Guide: How Connected Devices Improve Clinical Trial Data 5/29/2024

   Gain an overview of how and why connected devices provide sponsors and CROs with better clinical trial data, and offer patients much better trial experiences!

10. Minimizing Hurdles For Patients During The eConsent Process 10/4/2022

    Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.