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Contact : (321) 445-1969

Site Management

Site Management is a comprehensive relationship management with investigators and Clinical Research Coordinator (CRC) team along with management of all site documents and logs. GAP provides facilities like on-line site training and certification, study education and Good Clinical Practices (GCP) training to speed Institutional Review Board (IRB) submission and approval, and to facilitate patient selection, enrollment and randomization. We appoint highly qualified CRC at each study to assist and support the investigators and site staff with all study related activities, ensuring compliance with FDA, local regulatory and International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH)-GCP guidelines and an efficient completion of assigned duties.