Karen Crooks

This series of roundtable discussions will focus on key topics related to the challenges and opportunities faced by clinical trial sites in managing supplies. Each discussion group will provide a platform for sharing insights, discussing best practices and exploring innovative solutions aimed at optimizing the clinical trial supply chain processes.

How it Works: Choose a discussion you’d like to participate in. Each roundtable will be led by an expert facilitator. The session will consist of 40 minutes of group discussion, followed by a 20-minute feedback session

The discussion groups are:

GROUP A: Clarifying Site Roles in Clinical Trial Documentation: Defining Accountability and Responsibility

GROUP B: The Digitalization of Clinical Trial Sites: Now & Next.

GROUP C: Moving Forward: How Can Trial Sites Better Align With Supply Processes?