Clinical Research Support Center (CresCent)

The Clinical Research Support Center (CresCent in abbreviation) of the University of Tokyo Hospital provides assistance in the application and implementation of industry- and investigator-sponsored clinical trials in compliance with Good Clinical Practice (GCP) and other ethics guidelines. The center also serves as the Institutional Review Board (IRB) Office.

Site Coordinating Unit

The Site Coordinating Unit supports clinical trials and investigator-led clinical studies (voluntary clinical studies), and contributes to the early provision of advanced medicine to patients.

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Central Coordinating Unit

The Central Coordinating Unit supports the University of Tokyo Hospital in carrying out processes from the drawing up of protocols to the implementation/reporting of academia-sponsored clinical trials and voluntary clinical studies.

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Phase 1 Unit

The Phase 1 Unit (P1 Unit) was established by the University of Tokyo Hospital to safely and efficiently implement clinical studies in early development phase, with support of the Project for establishing a center for early and exploratory clinical studies (2011 to 2015) of the Ministry of Health, Labour and Welfare (completed May 2012).

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