Register today to attend eCOA/ePRO Digital Week, our free-to-attend webcast series designed to help (bio)pharmaceutical teams involved with ePRO/eCOA/PCOR stay on the pulse of evolving clinical technologies & strategies and enhance clinical trial efficiencies. This digital week provides benchmarking and shares practical case studies on the opportunities and challenges from increasing utilization of BYOD, mobile devices, sensors, wearables and other innovative technologies in clinical trial data collection. To learn about sponsorship of future events, contact

DAY 1 – SEPTEMBER 20, 2021

Why BYOD must follow patient choices, not outdated assumptions
9:00am EDT / 2:00pm BST / 3:00pm CEST

Although BYOD is becoming increasingly prevalent in clinical research, it is almost always viewed through a regulatory or technology lens, and not from the perspective of the patient. Sponsors often base their design decisions on misconceptions, such as the presumed unwillingness of patients to carry two devices. But the whole point of BYOD is not to make these kinds of assumptions.

In this session, attendees will learn why it’s crucial to follow patients’ choices, and explore best practices for building BYOD solutions that integrate seamlessly with patients’ lives, according to their individual preferences, behaviors, experiences and conditions.


Lisa Charlton
Senior Director, Product Development, eCOA
Science 37

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Is BYOD right for your eCOA Clinical Trial?
10:00am EDT / 3:00pm BST / 4:00pm CEST

  • Scientific, regulatory and operational considerations
  • Is BYOD really cost effective?
  • Current data on patient preference for BYOD versus a "provisioned" device
  • How to keep your patients engaged and compliant in a BYOD study


Celeste A. Elash
Vice President, eCOA Science

Chase Carmeans
Vice President, eCOA Operations

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Effective eCOA Oversight Strategies in Action
11:00am EDT / 4:00pm BST / 5:00pm CEST

  • Examine site and sponsor readiness for eCOA compliance oversight
  • Review current eCOA monitoring challenges
  • Managing monitoring and compliance challenges (difficult patients or sites, connectivity issues, backup approaches)


Joseph Im
Associate Director, Clinical Outcomes Assessment and Patient Innovations
Regeneron Pharmaceuticals

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DAY 2 – SEPTEMBER 21, 2021

Case Study: Practical Applications of Global, Decentralized Clinical Trials Within Highly Complex Therapeutic Areas
9:00am EDT / 2:00pm BST / 3:00pm CEST

When using sophisticated eCOA assessments, sponsors must capture both structured and unstructured data — on-site and remotely. Using the largest Alzheimer’s disease decentralized clinical trial to date as an example, this session discusses how remotely deployed data capture technology manages logistically and therapeutically complex clinical trials.

Key points:

  • How data were remotely collected from over 3,000 participants and caregivers via provisioned devices.
  • How the data platform managed complex cognitive assessments which required participants to draw cubes and other figures.
  • How a sophisticated eCOA collection solution integrated with other technology partners to simplify complex clinical trial deployment.


Jonathan Andrus
Chief Strategy Officer
Clinical Ink

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Developing a BYOD Implementation Framework for eCOA/ePRO
10:00am EDT / 3:00pm BST / 4:00pm CEST

  • How-to and logistics considerations for BYOD inclusion
  • Practical steps to building a BYOD framework
  • Sharing successes and challenges of BYOD implementation


Aman Thukral
Director, Clinical Systems and Digital Operations

Kelsey Linsmeier
Data Science Associate

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REGISTER NOW – Please select the webcast(s) you wish to attend and enter your contact details

Day 1

Day 2