Through highly experienced and skilled staff, 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

Training for research coordinators and monitors

Access to well-trained and experienced investigators QCR has worked with investigators who are experts in their field of study and have conducted numerous Phase I-III clinical trials both domestically and internationally. We can help you with the appropriate placement of investigators and staff to conduct clinical trials efficiently and effectively in order to bring a product to market.

 

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