- CIMeT has a Research Ethics Committee, a Research Committee, and a Biosafety Committee for the review of research protocols anywhere in Mexico.
In compliance with Good Clinical Practice guidelines and the current regulatory framework, our committees are autonomous in their operation and are integrated by highly qualified multidisciplinary personnel to evaluate and rule clinical studies on human beings to ensure that appropriate ethical and scientific conditions exist.
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Research Ethics Committee
Alberto Daniel Rocha Muñoz
President
Sonia Sifuentes Franco
Member Secretary
Sandra Lorena Muro Chávez
Member
Carlos Zúñiga Ramírez
Member
Antonio Gerardo Rojas Sánchez
Member
Eduardo Casillas González
Member
Jorge Eduardo Alvarado Aguilar
Member
Esteban González Díaz
Member
Abril Avalos Hernández
Representative of the Affected Nucleus
Research Committee
Luis Miguel Román Pintos
President
Cesar Arturo Nava Valdivia
Member Secretary
José David Medina Preciado
Member
Jhonatan Trujillo Quirós
Member
Alma Faviola Favela Mendoza
Member
Andrea Molina Pineda
Member
Misael Caballero Sandoval
Member
Biosafety Committee
Andrea Molina Pineda
President
Misael Caballero Sandoval
Member Secretary
Jorge Eduardo Alvarado Aguilar
Member
Esteban González Díaz
Member
Sonia Sifuentes Franco
Member
Sergio Ulises Zarate Reyes
Member
Our committees use ekomite®, an online system that enables a more effective and dynamic operation for project review to better serve the needs of researchers today and shorten response times.
If you wish to submit a research project to our committees, simply: login, register your project, upload the documents, and once the report is available, the system will inform you so that you can download all the stamped documents.
Research Participants
All biomedical research involving the participation of human beings must have the approval of a Research Ethics Committee conformed by professionals from different disciplines, in charge of ensuring the protection of the rights, safety, and welfare of subjects participating in a trial and of providing public assurance in this respect, through a decision on the trial protocol, the suitability of the investigators and the adequacy of the facilities, as well as the methods and documents to be used to inform the trial subjects in order to obtain their consent.
Before enrolling in a clinical study, the participant must receive full disclosure of all pertinent facts, including rights, risks, rewards, and obligations. This information is recorded in a document called the Informed Consent Form (previously reviewed and authorized by the committee). You can find all project-related information in the informed consent form, which you should have received a copy of. In the event of any concern, the researchers have the responsibility to provide information to the participant and to clarify all their concerns.
If you consider that your rights or welfare have been or are being affected by participating in a clinical trial, you may contact the Research Ethics Committee responsible for monitoring the study.
Want to listen to you!
Send us your questions or comments via the following form.
Contact:
Dr. Kevin Alexander González Godoy
Secretary Committees
- +52 33 3986 8280
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