Reduce the cost of clinical trials through improved site management, subject recruitment, monitoring and retention
One of the major challenges that Wipro bridges for clients conducting clinical trials are costs related to site management, subject recruitment, monitoring and retention. Our S-Trials platform uses digital technologies such as mobility, analytics, social, cognitive, UI/ UX and collaborative tools to ensure gaps are addressed and trial costs controlled. S-Trials improve outcomes through study-specific microsites, timely analytics about progress, predictions of performance and a sharp attention to study-related complaints from investigators and subjects. The platform supports Electronic Trial Master File (e-TMF), out of the box configuration to receive essential documents from sites based on the DIA Reference Model, Adverse Event submissions, integration with CTMS, CMS, DMS, EDC and RDC, and complete audit capabilities.
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