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ETCURAE IS THE SITE MANAGEMENT ORGANIZATION FOR CLINICAL RESEARCH WITH GREATEST REACH IN LATIN AMERICA, WE DEVELOP AND MANAGE WORLD CLASS CLINICAL RESEARCH SITES IN COMPLIANCE WITH THE MOST STRICT NATIONAL AND INTERNATIONAL REGULATIONS.

We operate and invest in the necessary infrastructure to develop highly specialized clinical research sites inside public health institutions.

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“We are the Site Management Organization with greatest reach in Latin America”

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YOU CAN TRUST US

We are one of the few organizations in Latin America that have the experience of working in compliance with the most important regulatory agencies in the world, to ensure excellence in clinical research.

WE ARE FOR

PATIENTS FIRST

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Our priority is to improve healthcare for patients, and we do so by enabling access to new and better treatments through clinical research.

WE VALUE OUR

INSTITUTIONAL ALLIES

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We help our institutional allies create a competitive and world class research platform at zero cost to attract clinical trials that benefit the advancement of science with new treatment options to benefit patient care.

WE ARE FOR

QUALITY FOR OUR SPONSORS

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We guarantee to our sponsors the most efficient processes and the highest quality results in compliance with national and international regulations.

What makes us different?

Everything.

We are an innovative model, we impact infrastructure and drug development in public health institutions, which enables access to treatment for all, but most importantly we strive to improve the patient’s quality of life.

As an organization we offer strategy, experience and investment in all the areas required for managing a research site in the most productive and efficient way.

Centralized project contracting across our site network

Strict quality management processes

Integrated service expertise

Access to a large and qualified patient base, including rare and orphan diseases

Strict project management processes

International regulatory compliance

Extensive experience in clinical research

Highly trained specialists in clinical trial execution

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What our partners & sponsors are saying about us

OUR TEAM

We pride ourselves with a team of deeply committed and passionate professionals, working alongside the best researchers and health-care professionals.

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Contact us!

Get in touch with us, whether you want to know more about our services, our on-going clincal trials or want to become a part of our institutional allies network, our team is ready to answer all your questions.

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About Us

Inspired by patient centric innovation & technology

Our hallmark is our continuous search for health technologies and innovative treatments that help improve health conditions for the population.

We develop and execute clinical trials with the highest quality standards in compliance to national and international regulations with clear objectives in the best clinical research sites.

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OUR MISSION

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Democratize and enable access to new health technologies through sponsored clinical research, to improve the patient’s quality of life.

OUR GOALS

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Provide our institutional allies with infrastructure, qualifications, training, technical and administrative support for them to actively participate within international research circuits that benefit patient care and tend to institutional priorities, positioning them as world class research sites.

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Provide our sponsors with quality research sites to conduct clinical trials efficiently in compliance with global regulatory agencies.

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Accelerate clinical research development through the use of data and innovative technologies.

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ETCURAE

OUR VISION

To become the most important site management organization for clinical research with global impact in Latin America.

HOW DO WE ACCOMPLISH OUR GOALS?

We support public health institutions with infrastructure, training, qualifications, technical and administrative support to conduct clinical research that benefits their patients with global quality standards in order to create a global and competitive clinical research platform.

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PATIENTS

Inspired by their impact in the future of medicine.

Our mission is to enable access to new and better treatments through clinical research to improve the patient’s quality of life.

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We enable access to more, newer and better treatments for patients with special needs of treatments, orphan diseases or without treatment options. We empower volunteer patients with all the information they need about their participation in a clinical trial.

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Our primary focus is care and control of patient safety.

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We ensure surveillance and continuous improvement of the patients’ experience.

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Total transparency.

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Our highly trained staff guarantees the best care for the volunteer patients.

The purpose of clinical trials is to find ways to more effectively and safely prevent, diagnose, or treat disease.

Many different types of people take part in clinical trials.


Some studies include healthy volunteers, while other studies include patient volunteers. Some studies include both healthy and patient volunteers.


Each study must include only people who meet the requirements for that study. These are the study's eligibility criteria, which determine who can participate in a clinical trial.


Any patient that voluntarily wishes to contribute to the clinical trial and that meet the eligibility criteria can participate in a clinical trial.


Eligibility criteria are different for each trial. They include whether you are a healthy or patient volunteer. They also include factors such as your age and sex, the type and stage of disease, and whether you have had certain treatments or have other health problems.


The criteria ensure that new approaches are tested on similar groups of people. This makes it clear to whom a clinical trial's results apply.


Eligibility criteria are not used to reject people personally. Instead, the criteria are used to identify appropriate participants and keep them safe, and to help ensure that researchers can find the new information they need.

Clinical trials offer hope for many people, while giving researchers a chance to find treatments that could benefit patients in the future.


Healthy volunteers say they take part to help others and contribute in the advancement of science. People with an illness or disease may take part to help others, but also to have a chance to receive the newest treatment and get added care and attention from the clinical trial staff.


Clinical trials may involve risk, as can routine medical care and the activities of daily living. When weighing the risks of clinical trials, consider the possible harms that could result from taking part in the trial, the level of harm, and the chance of any harm occurring.

It is important to acquire as much knowledge about the clinical trial as possible before being part of it. You should make sure to have all your doubts answered by the members of the team that will be doing the trial. Also, you should mention the trial to your main health provider to confirm that the trial is a viable option for you considering your current treatment.

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COFEPRIS – Comisión Federal para la Protección Contra Riesgos Sanitarios https://www.gob.mx/cofepris

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CONBIOETICA -- Comisión Nacional de Bioética https://www.gob.mx/salud/conbioetica

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NHLBI – National Heart Lung and Blood Institute - U.S. Department of Health and Human Serviceshttps://www.nhlbi.nih.gov/health-topics/clinical-trials

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FDA – Administración de Drogas y Alimentos–https://www.fda.gov

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NIH - Institutos Nacionales de Saludhttps://www.nih.gov

All clinical trials must be registered and are strictly regulated by a legal framework composed of laws, guides and regulations. In México they must be compliant with the General Health Law and Official Mexican Standards; as well as compliance with international guidelines (FDA guidelines, Declaration of Helsinki, Good Clinical Practices, etc.).


For more information on regulatory compliance of clinical trials click here.


The purpose of these strict regulations is to protect whoever participates in clinical trials and to ensure that the information obtained from the studies is reliable and can be used to benefit the community.


Even though there are many efforts made to avoid any potential risks to the participants during the investigation, there are some that can occur which can’t be avoided since clinical trials involve ongoing investigation of the treatments from which we are still learning and trying to perfect.


This is why volunteer patients should only be part of a clinical trial once they have full knowledge of what the trial entails, it’s advantages and possible disadvantages. Once the volunteer patient has complete knowledge of the trial, they should be asked to sign an informed consent.

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Advantages of a clinical trial:

Possibility to receive a new treatment for a disease before it is widely available.

You take part in helping others to have a better treatment for their diseases in the future by aiding the development of a new drug.

Part of your treatment may include more regular health check-ups.

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Possible disadvantages of a clinical trial:

The new treatment you receive may have cause side effects.

The new treatment received may not be more efficient than the existing treatment or may not work or you.

There’s the possibility that you are NOT part of the group that receives the new treatment, you could be placed in the control group, meaning you would receive what already exists as treatment or a placebo.

To be part of any clinical study you must meet all the requirements of the eligibility criteria. If you want to find out if you are eligible for on-going clinical studies within our network of institutional allies, please fill out enquiry form in the contact section, so you can receive further information.

Click on the links below to learn more about the on-going clinical trials in your area.


Please Fill our an enquiry form in the contact section so you can receive further information of the clinical trials EtCurae is performing within its site network.

MEXICO

Comisión Federal para la Protección contra Riesgos Sanitarios – Consulta de Ensayos Clínicos Registrados

INTERNATIONAL

National Institutes of Health – U.S. National Library of Medicine – ClinicalTrials Data Base

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INSTITUTIONAL ALLIES

Together, let’s drive innovation that improves patients’ lives.

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We invest in creating optimal conditions to develop clinical research sites, with infrastructure and state of the art technology for the benefit of patients at a zero cost for our institutional allies.

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Within a transparency framework and with the best practices, we create scientific synergy to boost global health innovation, attracting the largest number of high-impact clinical trials to our institutional allies.

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As an institutional ally, you obtain greater visibility globally on high impact clinical research.

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High efficiency in clinical trials with rigorous compliance in Good Clinical Practices.

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Regulatory compliance with the most important agencies globally.

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Active participation of researchers, medical doctors, nurses and health professionals from the institution on clinical trials.

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Researchers have the possibility of participating as co-authors in scientific publications.

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High-specialization of research teams and training for international regulatory compliance, all sponsored by EtCurae.

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Volunteer patients benefit from having access to more, new and better treatments free from charge.

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As an institutional ally, you obtain data and intelligence for strategic decision making, to optimize resources and streamline processes.

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Participating efficiently in global clinical trials reinforces regulatory compliances, it increases attention means and patient care.

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Through participation in clinical trials it is possible to generate resources to improve, renovate or increase attention means for patients.

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SPONSORS

Inspired by

Our clinical trials deliver maximum quality and efficiency, the best practices and rigorous compliance with global regulatory agencies, ensuring total data integrity, transparency and safety for patients.

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We offer a wide range of integrated services for research and development.

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Access to a large and qualified patient base, including rare and orphan diseases.

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Access to a wide range of specialties.

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Access to a research site network to guarantee clinical trial feasibility.

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Infrastructure capable of supporting clinical trials phase I, II, III and IV.

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Close collaboration with public health institutions.

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Quality assurance compliant to the most rigorous standards and the most important regulatory agencies.

Site Management

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Centralized project contracting

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Site selection within SMO network

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Site administrative processes

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Site preparation

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Investigator preparation

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Quality Management on the site

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Quality Control on the site

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Drug control for studies

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File control for studies

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Management and attention of audits

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Co-ordination with all service units within sites and in between sites

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Patient recruitment and retention strategies

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Central laboratory within SMO sites

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Centralized patients’ database

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Data analytics of: Patients, Investigators, Capacity, Geography Distribution, Diseases.

Project Management

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Our project managers and site coordinators will maintain a close follow-up with internal departments and communicate with the sponsor and institutional partners transparently on project updates at all stages of project execution.

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Our expertise includes:

Project managers with hands-on experience.

Single point of contact for accountability.

Therapeutic area experts.

Trained on GCP.

Global regulatory experience.

Predefined Risk Mitigation strategies

Quality Assurance

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We ensure adherence to our customer’s requirements and applicable global regulations such as COFEPRIS, FDA, EMA, ANVISA, ISP-Chile, INVIMA, MHRA and others. Our services comply with Good Clinical Practices (GCP), Good Laboratory Practice (GLP) and the International Conference on Harmonization (ICH). Our promise to continuous quality allows us to create a strong system of corrective and preventive actions (CAPA). Our team investigates deviations, discrepancies, incidents, etc., and works proactively to detect, correct and prevent actions in time and with accurate documentation.

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Centralized project contracting

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Site selection within SMO network

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Site administrative processes

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Site preparation

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Investigator preparation

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Quality Management on the site

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Quality Control on the site

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Drug control for studies

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File control for studies

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Management and attention of audits

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Co-ordination with all service units within sites and in between sites

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Patient recruitment and retention strategies

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Central laboratory within SMO sites

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Centralized patients’ database

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Data analytics of: Patients, Investigators, Capacity, Geography Distribution, Diseases.

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Our project managers will maintain a close follow-up with internal departments and communicate the sponsor and institutional partners transparently on project updates at all stages of project execution.

health

Our expertise includes:

Project managers with hands-on experience.

Single point of contact for accountability.

Therapeutic area experts.

Trained on GCP.

Global regulatory experience.

Predefined Risk Mitigation strategies.

health

We ensure adherence to our customer’s requirements and applicable global regulations such as COFEPRIS, FDA, EMA, ANVISA, ISP-Chile, INVIMA, MHRA and others. Our services comply with Good Clinical Practices (GCP), Good Laboratory Practice (GLP) and the International Conference on Harmonization (ICH). Our promise to continuous quality allows us to create a strong system of corrective and preventive actions (CAPA). Our team investigates deviations, discrepancies, incidents, etc., and works proactively to detect, correct and prevent actions in time and with accurate documentation.

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REGULATORY COMPLIANCE

Committed to comply with the highest regulatory standards

As a Company dedicated to clinical research of the highest quality, EtCurae strictly complies with all the policies and laws regrarding health research and personal data protection that follow:

health General Health Law. Article 100 Download
health Bylaw of the General Health Law regarding Health Research. Download
health NOM-012-SSA3-2012: Policy that establishes criteria for the conduction of health research projects in human beings. Download
health National Guide for the Integration and operation of Research Ethics Committees, National Bioethics Comission, Sixth Edition, 2018. Download
health NOM-004-SSA3-2012: Policy of Medical Records. Download
health World Medical Association Deeclaration of Helskinki – Ethical Principles for Medical Research Involving Human Subjects. Download
health Good Clinical Practice of the International Council for Harmonization ICH-E6-R2. Download
health Federal Law of Personal Data Protection in Possession of Privates. Download

If you have questions or wish to speak personally with our team of experts, we are ready to answer all your inquiries.

Call us at: +52 (55) 4124 0234 Extension 011

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WE ARE

Inspired by patient centric innovation & technology

We provide maximum efficiency and quality in the execution of clinical research tailored to specific needs.

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01. OUR MISSION

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We are for our patients enabling access to new and better treatments, inspired by their impact in the future of medicine.

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We are for our sponsors taking innovation forward.

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We are for our partners providing the best conditions to attract clinical trials and improve patient care.

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We are for taking health forward!

our primary objectives

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To democratize and enable access to new and better treatments for patients in Latin America through clinical research.

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To position our institutional partners as international research institutions.

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To accelerate clinical research development through the use of data and innovative technologies.

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ETCURAE

02.   OUR VISION

To become the most important site management organization in America with global impact.

HOW WILL WE ACCOMPLISH OUR GOALS?

We support the Institutions and Research Centers where we participate in the construction of structures and mechanisms that empower them to conduct clinical research activities that benefit patients in the most agile and safe manner with global quality standards, boosting their profiles to create a clinical research platform competitive worldwide.