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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 |
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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 Regulatory agencies consider safety to be of primary importance
in the conduct of a clinical trial. QCR has experience in
setting up first-rate safety surveillance systems to ensure
that your data is being monitored according to GCP/ICH guidelines
and that safety event reporting is compliant with FDA regulations.
We can offer services such as safety infrastructure development,
adverse event review and coding, and preparation of IND safety
reports. |
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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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