Transforming How Sponsors and CROs Interact with Clinical SitesMarch 31, 2017
Clinical trials are expensive. With the constraints of quality and compliance, the only way to reduce costs is to make trial operations more efficient. When study sponsors are able to automate workflows and efficiently exchange information, documents, queries, and supplies with their clinical sites, good things happen: confusion and errors are minimized, relationships with investigators and site personnel improve, and overhead costs plummet.
Join Param Singh, director of clinical operations solutions at Perficient, for a 30-minute on-demand webinar, in which he discussed how organizations can use strategy, technology, and design to reduce clinical trial costs while improving quality and compliance.