Additionally, but not least, we understand the importance of the finalization, return and filing of the normative documents of the sponsors, required by the regulatory agency, the IRB, the pharmacy, the laboratory, the hospital and the related entities, therefore we have specialized personnel in the handling and protection of data to ensure the complete completion of the documents and supervise the continuous regulatory compliance of the same until the closure of the 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.Contact Us
Sur 132 No. 108 Suite 601-605 Col. Las Americas CP 01120
Phone: 52(55) 2614 5118
52 1 55 733805117
Cdla. Los Ceibos, Los Olivos 3, Av. Leopoldo Carrera Calvo #103 y calle 15va Edif, EBC
Phone: +593 04 507 5777