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Clinical Trials Toolkit Series: Clinical Research Systems: Vestigo®️, eReg™️, & WVU+kc (updates)

WVCTSI will host its next Clinical Trials Toolkit session on Friday, Oct. 15 from noon to 1 p.m. in person or via remote connection. The presentation will focus on Clinical Research Systems: Vestigo®️, eReg™️ & WV+kc (updates) in person or via remote connection.

Part One: Elizabeth Berry-Bartolo, Pharmacy Specialist, Investigational Drug Services from WVU Inpatient Pharmacy will provide an overview of how VESTIGO®️ has transformed Investigational Drug Service (IDS) by automating manual processes associated with IDS management and operations. The advantages of using VESTIGO®️, including increased safety, efficiency, compliance and accountability will be discussed.

Part Two: Gretchen McMasters, Director of Office of Human Research Protection and Jessica Williams, Assistant Director of Office of Human Research Protection will be providing updates on recent changes at the Office of Human Research Protections (OHRP) such as IRB submission system status, SOPs, data protection form, eIC, build forms, etc.

Part Three: Anya Slaven, Regulatory Systems Analyst, WVCTSI CT Center of Excellence will present this session on how to use eReg™️ to help with organizing and maintaining research study documentation but also to comply with FDA regulations and documentation guidelines for good clinical practice (GCP).

Please direct any questions regarding the presentations to Kerri Rogers at