How digitized protocols are accelerating clinical research

Digitizing clinical trial protocols is essential for accelerating research, enhancing data accuracy and compliance, reducing costs and improving patient recruitment through optimized trial designs. It enables better collaboration between AI and human expertise, marking a shift toward modern, data-driven clinical research that advances medical science and improves patient outcomes. 

However, sponsors face challenges in effectively digitizing trial protocols, including complex workflows, data integration, regulatory compliance and data security. This white paper addresses these challenges and outlines ways to successfully implement and maintain digitized protocols.

There are two case studies in this paper:

• Applying AI and human intelligence (HI) to leverage digitized protocols in medical writing
• Real-world EMR data informs protocol design