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:

	Clinical research infrastructure development
	Research site assessment and preparatory study development
	Strategic consulting
	Project management for research site coordination and oversight
	Liaison with industry, government and other institutions
	Safety monitoring
	Clinical monitoring
	Development of research plans and reports including proposals, timelines, protocols, consent forms, CRFs, SOPs
	Medical writing
	Preparation of presentations to IRBs, DSMBs, FDA, and other international institutions QCR has extensive experience in the preparation and delivery of important presentations to research bodies, regulatory agencies, oversight committees, and community representatives.
	Training for research coordinators and monitors
	Access to well-trained and experienced investigators