By Crista Casey, VP of Clinical and Regulatory Operations
First and foremost, patient safety is paramount.
Transitioning from pre-clinical to clinical trial work is an exciting time; ripe with adventure and possibilities. During this time, program level planning increases in detail and structure while individual projects take shape. Deliberate flexibility in program and project planning allows trials to excel in areas like regulatory submission and approvals, enrollment and retention, and data review. Simple language adjustments to the protocol, intelligent use of decentralized services and real time data visibility via intuitive technology like encapsia can reduce project timelines by weeks or even months.