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Through highly experienced and skilled staff, Quattro Clinical Research (QCR) provides the following clinical research services to evaluate vaccines, therapeutics and devices both domestically and internationally:
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Clinical research infrastructure development |
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Research site assessment and preparatory study development |
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Strategic consulting QCR can provide consultation to develop strategic plans for
conducting clinical research including forecasting and tracking
of clinical development timelines and milestones. With our
global experience, QCR can provide consultation on the most
efficient and effective means to initiate a clinical trial
in domestic and international settings. Let us help you connect
with the appropriate offices and agencies to ensure a smooth
start to your trial. |
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Project management for research site coordination and oversight |
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Liaison with industry, government and other institutions |
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Safety monitoring |
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Clinical monitoring |
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Development of research plans and reports including proposals, timelines, protocols, consent forms, CRFs, SOPs |
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Medical writing |
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Preparation of presentations to IRBs, DSMBs, FDA, and other international institutions |
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Training for research coordinators and monitors |
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Access to well-trained and experienced investigators |
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