COVID-19 has prompted a greater need to keep existing clinical trials on track by enabling digital processes and remote access for study monitors. Learn how research sites have changed decade old paper-based processes and implemented remote monitoring and digital processes within days. They will share lessons learned and practical advice for how sites can improve their operations and keep research moving forward.

Objectives:

• Review real-world case studies from clinical research sites and insights gained from going digital and adopting electronic signatures.
• Receive guidance for updating SOPs and best practices for granting remote source access to monitors.
• Explore considerations from other sites when evaluating new technology.