WS23.2 – Blinding in Clinical Trials (B)

This beginner level workshop provides a comprehensive overview of blinding in clinical trials, focusing on its critical role in minimizing bias and ensuring data integrity. Participants will learn about various blinding methods (single, double, and triple blinding), practical implementation challenges, and strategies to maintain blinding throughout the study. The session also covers regulatory expectations and real-world scenarios where blinding may be compromised. Designed for clinical operations, study managers, and quality assurance professionals, this workshop equips attendees with the knowledge to design and manage effective blinding processes.