BRCR Global has the capability to provide advice for the preparation of the containing document of the entire clinical research strategy of a medicine, which describes the clinical studies that will be carried out for a pharmaceutical entity or subsidiary, in order to maximize the quality of the data.
BRCR Global is a CRO that offers and adapts itself in an individual way to a plan design for an active substance, device, procedure or a specific treatment strategy, with the purpose of presenting the study data as part of a request for authorization of marketing to the FDA. This plan would indicate the correct decision points and would allow modifying any variable through the process evolution.
We have extensive experience in a variety of therapeutic areas by managing studies in USA, Latin America, Caribbean Islands and Central America. We have built strong business relationships with main researchers in several cities in the referred regions.
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