eConsent & Modern ICFs: Balancing Innovation and Ethics
Join industry leaders from RWS and Pfizer as they delve into the evolving landscape of Informed Consent Forms (ICFs) and how they’re being reimagined to better serve patients and meet global regulatory standards. This insightful webinar will explore how organisations can create ICFs that are not only compliant but also clear, culturally sensitive, and truly supportive of informed decision-making.
Discover how global teams are responding to regulatory frameworks like the EU Clinical Trial Regulation (EU CTR) and FDA guidelines while maintaining consistency and clarity across diverse markets. Learn from Pfizer’s collaboration with RWS and gain practical insights into improving the quality, readability, and digital readiness of your consent materials.
Whether you're involved in clinical operations, regulatory affairs, or patient engagement, this session will equip you with actionable strategies to enhance your ICF processes and outcomes.
Key Takeaways:
- Practical strategies for writing and reviewing plain language content.
- Best practices for multilingual translation and cultural adaptation of ICFs.
- Insights into implementing eConsent and digital delivery workflows.
- Tips for aligning internal stakeholders across clinical, regulatory, and patient engagement teams.
Good news: This is a virtual event that can be attended from the comfort of your office/home, eliminating the need to travel. By choosing to attend this virtual event, you are contributing to a more sustainable future while still benefiting from valuable industry insights.
