In this free webinar, gain insight into the current landscape of “Bring Your Own Device” (BYOD) adoption across therapeutic areas and geographies. Attendees will learn about the key technical and regulatory risks tied to device variability and offline data capture. The featured speakers will discuss how BYOD affects patient recruitment, retention and compliance — and whether it introduces new accessibility challenges.
TORONTO, Sept. 22, 2025 /PRNewswire/ — The promise of “Bring Your Own Device” (BYOD) in clinical trials has sparked equal parts excitement and skepticism across the research community. Supporters point to greater patient convenience, faster recruitment and potential cost savings. Critics raise concerns about data integrity, regulatory acceptance and technology disparities. So — where does the truth stand?
In this webinar, the featured speakers will move beyond the buzzwords and dig into the real-world evidence shaping BYOD adoption in ePRO and eCOA studies.
The expert panel will explore:
- The State of BYOD in Clinical Trials – Understanding adoption trends, identifying therapeutic areas where BYOD thrives and confronting its current limitations
- Data Quality & Integrity – Addressing device variability, OS updates, offline data capture and how to meet regulatory expectations without sacrificing flexibility
- Patient-Centricity: Promise vs. Reality – Reviewing whether BYOD truly improves recruitment, retention and compliance — or if it widens the accessibility gap
- Regulatory & Privacy Considerations – Navigating HIPAA, GDPR and global frameworks, informed consent requirements and the critical role of submission screenshots
Sponsors, CROs, technology providers and clinical operations professionals will gain clarity on separating hype from reality, understanding the evolving regulatory landscape and evaluating if BYOD is the right fit for upcoming trials.
Register for this webinar to learn how BYOD in clinical trials is shaping data quality, patient engagement and regulatory strategy.
Join Megan Petrylak (Moderator), Chief Operating Officer, Clinical ink; Vicki Gashwiler, Global Head, Clinical Operations, ProPharma; Clare Campbell-Cooper, Global Head of Digital Health and Innovation, Fortrea; Guy Crossley, CEO, Quokka Care; and Karen Lynn Søndergaard, MSc, PhD, Senior Clinical Operations Lead, Novo Nordisk A/S, for the live webinar on Tuesday, October 7, 2025, at 11:30am EDT (4:30pm BST/UK).
For more information or to register for this event, visit BYOD or Bust: Are Clinical Trials Ready for the Device Revolution?
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