ePRO Resources

1. ePROM Implementation: 4 Best Practices For System Functionality 2/13/2024

   Explore four of the 15 system functionality considerations highlighted in an eCOA Consortium article that aim to create a more thorough and standardized approach to ePROM implementation.

2. Designing ePRO And eConsent For Pediatric Trials 8/29/2024

   Gain confidence in making your next pediatric trial more successful by leveraging the technology discussed to address common challenges in pediatric studies.

3. The Building Blocks Of DCT: How To Create A Seamless Experience Across eConsent, eCOA, And More 3/29/2022

   With more than 76% of sponsors seeking to implement decentralized solutions this year, there’s never been more attention given to decentralized trials. Discover why decentralized trials must take a unified approach, one that alleviates burdens for patients and sites in order to drive cost savings and realize efficiencies. 

4. Leveraging Tech And Clinician Review To Improve Risk Detection 10/19/2023

   Learn why neuroscience therapy developers should start adopting strategies to improve data quality and assess responses using a combination of technology and expert clinician review.

5. Paper vs. eCOA: Hard Calculations For Easy Decisions 6/13/2023

   Sticker prices often guide purchases, but there's a broader perspective that encompasses total cost. Use this calculator to compare prices of paper COAs or eCOAs, including ePROs, eDiaries, and eClinROs.

6. Training Program Reduces Placebo Effect By More Than 50% In ePRO Study 5/17/2023

   Discover how an instruction program directly contributed to significantly lowering the placebo response rate in a phase III migraine CNS study.

7. Why ePROs In Oncology Are Perfect For Capturing The Patient's Voice 5/15/2025

   Recently released FDA guidance showcases why electronic patient-reported outcomes (ePROs) are ideal for capturing the “voice” of the patient. See how ePRO eases oncology trials.

8. An ePRO Platform Designed With Real People In Mind 4/6/2023

   With a combination of technology and consultative support from team experts, start experiencing a seamless ePRO transition and establish a smoother path to regulatory submission today.

9. Regulatory Guidance For PRO Strategy In Oncology Trials 11/10/2023

   Kelly Dumais, Principal Scientific Advisor, and Jowita Marszewska, Scientific Advisor at Clario eCOA, delve into the specifics of how recent regulatory advancements are influencing PRO Strategy.

10. Safety Monitoring: What Does ePRO Have To Do With It? 1/10/2022

    In the available blog post, learn about the importance of safety monitoring in clinical trials.