How Site-Based eSource Benefits Sponsors by Boosting Site Success

eSource is the only data repository that documents protocol and GCP compliance, patient safety, and directly integrates clinical care and research. Sponsors can promote better outcomes and help improve data precision by encouraging site-based eSource across their participating sites. It is a widely held, but false belief that sites currently use electronic health records (EHR) for source data collection, but they don’t.

Historically, sites have used error-prone paper, but over the last decade, maturation of the research site industry has driven a shift towards adoption of site-based eSource. With built-in quality up front, site eSource opens up radical new ways of reorganizing monitoring and data management workflows to improve efficiency and data quality.

Register for this webinar and join the featured speaker, to unravel the myths about site-based eSource, and understand the downstream efficiencies to sponsors and CROs.

Speaker

Raymond Nomizu, CEO & Co-Founder, CRIO

Raymond Nomizu is the Co-Founder and CEO at CRIO, an eClinical provider for sponsors, clinical research organizations (CROs) and sites. CRIO’s system allows research sites to collect data accurately and contemporaneously, and sponsors to view the data in real-time, without costly source data verification. Prior to founding CRIO, Raymond owned and operated an independent clinical research site, co-founded a real estate data analytics firm called Bench Core (later sold) and served as a Management Consultant both independently and as a Principal for The Boston Consulting Group. He has over 10 years’ experience consulting senior management across multiple industries on issues of business strategy and process improvement. Raymond has AB and JD degrees from Harvard University.

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