The clinical sites network in Mexico with 15 years of experience with five sites.


We collaborate in the search and development of innovative medical solutions to contribute to a better quality of life for patients. We want to be an international benchmark in clinical research and medical care by developing leaders who diversify and innovate. We conduct clinical trials supported by standard operating procedures because of the implementation of the Quality Management System and based on ISO 9001:2015 standards. We formalize the recruitment, selection, and registration of subjects through standardized processes with the broadest ethical sense and in full adherence to national and international standards.

Mexican Population: 126 millions and many race: Indigenous Afroamerican.
We have conducted more than 100 clinical trials
ISO 9001-2008
Standardized processes


Patients recruitment in short period on time
Multi ethnic population
Large numbers of patients with different illnesses
The only netwok with five sites in Mexico

Main Therapeuctic Areas

  • Cardiology

  • Oncology

  • Pediatric Cardiology

  • Dermatology

  • Pediatric Endocrinology

  • Gastroenterology

  • Geriatrics

  • Gynecology

  • Hematology

  • Traumatology

  • Infectious Diseases

  • Internal Medicine

  • Family Medicine

  • Nephrology

  • Pneumology

  • Neurology

  • Pediatrics

  • Ophthalmology

  • Odontology

  • Rheumatology

Qualified to conduct Phase I*, II, III and IV studies.
*Only in Oaxaca

National and International Audits

National audits by Sponsor Cofepris inspections International Audits Certification Audit
  • Sanofí
  • Regeneron
  • CanSino
  • Celltrion
  • 1 TPUS 13
    (Gastric Cancer) 2013
  • 1 CanSino / Nov. 2020
  • 2 Chinese government /Feb. 2021 (CanSino)
  • 3 to ISO 9001-2008


Institutional Review Board
Biosafety Committee
Research Committee

They are permanent and evaluative; they are responsible for reviewing, issuing reports and making recommendations based on good clinical practices regarding clinical research activity. Its operating procedures ensure that the dignity, rights, safety and well-being of the subject participating in a research study are safeguarded.

  • Electronic submissions

  • Review and request for changes in five days (if necessary)

  • The response time from the Committees is less than ten working days

Start Up Coordination

a) Feasibility Area

We have an area specialized in carrying out the feasibility of all the centers in the network.

b) Regulatory Area

We have an exclusive area to streamline the regulatory procedures between Ethics Committee and Sponsor.

Response Times

The response time for feasibility studies is no more than five working days.
Sending the package for submission to COFEPRIS in no more than twenty four working days.
The contractual part can be elaborated in parallel to the initial submission, with an average response time of less than five working days.


  • Ambient Centrifuge

  • Frozen Centrifuge

  • -20ºC and -80ºC refrigerators

  • Refrigerator from 2º to 8º with continuous monitoring thermometer

  • Laminar Flow Hood

  • Biosafety Hood

  • Equipped Infusion Rooms

  • Clinical Archives with Controlled Access

  • Dead File Controlled Access

  • Pharmacies Controlled Access

  • Medical Emergency Trolley

  • Shock Area

  • Emergency Power Plant

  • Immunohistochemistry Equipment

  • Breast Panel

  • Hormone Receptors

  • HER2

Human Resources

190 collaborators in Red OSMO


  • Local Laboratory

  • Hospital for Adverse Event Care

  • Medical Imaging

Developed Projects

APOLO project

A special project of the Start Up area that seeks to increase the researcher pipeline.

Central Laboratory for PBMC Procurement in Mexico

We are the only site in Mexico that can perform the PBMC purification process.

Mobile Nursing

Home medical service supported by the mobility infrastructure generated during the pandemic.

Hospital in Oaxaca

(Integral Health System)

Research Protocol Management System (ERP)

First integral software in Mexico specialized in the conduct of clinical trials.

Marketing focused on Recruitment

Socializing Clinical Research as a therapeutic alternative
Recruitment focused on objectives
Digital Ecosystem for Recruitment
Social Responsibility Actions
*Thanks to clinical research, one day we will beat cancer

Strong international partnerships