Across Your Entire Portfolio
Building a stand-alone, fully functional IRT system for every clinical trial study is not necessary, but without one, you may be forced to run your Phase I, IV and Investigator Sponsored Trials manually. DRIVE delivers the benefits of IRT supplies management to your entire development program in one system, enabling automated IRT-like supply functionality that minimizes costs, reduces waste and helps you manage regulations across sites.
The Benefits of DRIVE
The DRIVE system allows sponsors and sites to manage a trial at the program level. The system performs tasks like managing drug expiration, monitoring pooled supplies and IRT protocols, and screening country and site sourcing in real time.