Conducting a trial with a sponsor of choice is more important to sites than ever. See how a pharma company reduced investigator payment cycle time by 55 percent while decreasing their own administrative burden by 90 percent in this metrics-rich case study.
When patient consent must be obtained at home or in the hospital, monitoring compliance can become a time-consuming procedure for sites and sponsors. There is a better way! Learn more in this 30-minute on-demand webinar.
Sponsors, CROs, and sites are pivoting and adjusting to an environment requiring study start-up and conduct to be much more remote. Find out how to use multifunctional study portals effectively to minimize disruptions to trial operations.
With a centralized training catalog and cross-trial credits, the IQVIA LMS (Learning Management System) module of the Investigator Site Portal eliminates redundant work for both sites and study teams, making trials more efficient for everyone.