Talk Clinical Trials Innovation track
S0102 - Patient Involvement During the Lifecycle of Clinical Trials
Wed, Mar 19, 2025 · 8:30–9:40 AM CET Delhi Room, Congress Center Basel
About this session
This session will explore concrete actions to enhance patient involvement at different time points throughout the clinical trial life cycle. Through a multistakeholder discussion, it will cover key aspects such as integrating patient perspectives in trial design and operations, industry approaches to patient engagement, and improving informed consent processes to ensure better comprehension and accessibility.
Programme:
- 3. Generating a New Informed Consent Form Template via a Co-Creation Process: From a Legal to a Comprehensible Document — Evelijn Zeijdner
- 2. Industry perspective on reflecting patient involvement in clinical trials — Cathelijne de Gram
- 1. Patient Involvement During the Life Cycle of Clinical Trials — Monique Al
- Panel Discussion — Evelijn Zeijdner, Monique Al, Marina Malikova, Cathelijne de Gram
- 4. Developing and Implementing Strategies for Patient-Centric Biomedical Product Development — Marina Malikova
Speakers
-
Executive Director of Research, Assistant Professor of Surgery · Boston University School of Medicine
Speaker
-
Director EU Global Regulatory and Scientific Policy, Global Regulatory Affairs · Merck BV
Speaker
-
Patient Engagement in Research Coordinator · Hospital Sant Joan de Déu Barcelona
Chair
