Explore why patient engagement is the cornerstone of successful rare disease trials, emphasising the importance of designing studies around the realities of patients' lives to build trust and improve outcomes.

Discover how thoughtful design, clear language, and structured visuals can transform overwhelming side effect information into accessible, actionable insights for patients in our latest Health Literacy series.

Caregivers are vital to clinical trial retention, yet often overlooked—this article highlights their challenges, impact, and how to better support them.

Discover the key trends shaping clinical research in 2026, from patient-centric approaches to empowering site staff and fostering stronger human connections.

Discover how clear communication and health literacy principles can transform complex patient materials into simple, engaging, and empowering health information.

Go behind the scenes of The participation equation – our call to put people, not just data, at the heart of clinical research.

In the final article of this series, we explore how education and communication can empower clinical trial participants to manage and report side effects confidently.

This second article in the series uncovers the mental and emotional toll of underreported side effects in clinical trials. Learn how unspoken burdens impact participant wellbeing, adherence, and data quality, and why addressing these challenges strengthens trial integrity.

This first article in a three-part series examines the disconnect between how patients and HCPs perceive and report side effects in clinical trials. Discover why these misaligned perspectives arise and how they impact participant quality of life, engagement, and trial outcomes.