INSTITUTIONAL RESEARCH BOARD (IRB)

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In accordance with the Good Clinical Practices and Mexican legislation, the Clinical Trials must be review by an Ethics Committee, a Research Committee and, in some cases, a Biosafety Committee. These review important aspects of the clinical trials, such as the methodology and design of the study, potential risks and possible benefits for the patient to above all safeguard the dignity, respect and safety of the participants within the research protocol.

COMMITTEE

 

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Currently all of our protocols are evaluated by the different committees of the Hispano Hospital, which have current registries according to the guidelines of Cofepris and Conbioetica.

Comité de Ética en Investigación de Investigación Biomédica para el Desarrollo de Fármacos S.A. de C.V.

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CONBIOETICA REGISTRY
14-CEI-006-20170504.

 

 

Comité de Investigación de Investigación Biomédica para el Desarrollo de Fármacos S.A. de C.V.
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COFEPRIS REGISTRY
17 CI 14 120 132.