Compliance with the protocols in which we take part is one of our priorities, therefore we have an extensive specialized and trained staff in each clinical research discipline, in addition to the most experienced and committed researchers, in order to provide the sponsors and CROs with reliable results, based on the PCBs and specifications of the protocols.
Each of our professional components (physicians, coordinators, statutory specialists, administrative and financial personnel, nurses, laboratory technicians and external suppliers) assumes the importance of their functions and obligations in the achievement of the specific objectives of the protocol and compliance of the specific criteria of success in the time established for each study.
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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