Clinical trial study startup processes are an area ripe for optimization. Often, the study time clock doesn’t start ticking until First Patient In (FPI), but research shows that the process to get to FPI can take seven months or longer on average.

This webinar will explore best practices for study startup with practical advice on how to reap the benefits of automating processes while increasing compliance. The featured speakers will discuss some common misconceptions around digital versus electronic signatures and provide advice on how to ensure all of those signed documents comply with US Food and Drug Administration (FDA) 21 CFR Part 11 guidance.

A speaker from Clinilabs Drug Development Corporation will share a case study on how they streamlined clinical trial startup processes, optimized their tools and cut clinical trial study startup times in half.