Home · Resources · Case Study University of Louisville Improves Regulatory Efficiency with Veeva SiteVault ? ? ? ? Lale Akca, MBA, CCRA, Executive Director of the Clinical Trials Unit at the University of Louisville, presents at Veeva R&D Summit. Clinical research sites, sponsors, and CROs fill the room at Veeva R&D Summit to hear how Lale Akca and Rachel Sheppard of the University of Louisville set out to transform their regulatory operations to promote efficiency and collaboration across their teams and study partners. With 150 active trials and 60 new studies in the pipeline across 30 specialties, the Clinical Trials Unit at the University of Louisville manages a complex research environment. A growing pipeline of clinical studies is a good thing for clinical research sites. But for sit

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