Highly efficient Clinical Research run by a team of dedicated professionals.

How We Work

1

We collaborate closely with our sponsors to develop investigation protocols that comply with
all relevant regulations, with the aim of obtaining approval from the relevant health authorities.

2

At the outset, we develop a comprehensive plan and a clearly defined budget.

3

Our database provides access to the statistical data gathered during the clinical study.

4

Our team is highly proficient in a wide range of EDC (Electronic Data Capture) systems.

5

We oversee the progression of clinical studies and have established procedures for the
compilation of all data collected.

6

We adhere to all legal and ethical compliance regulations.

7

We provide assistance in the analysis of data and the preparation of clinical research reports.

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We oversee all registration processes directly with

Our Organization

The Board of Directors

In accordance with international standards of corporate governance, we guarantee
transparency and accountability to the company’s shareholders, sponsors, and the general
public.

Office Services for Sponsors

To ensure the highest level of service, we have implemented a direct management system to
address the specific needs of our sponsors.

Given the complexity of the regulations governing clinical studies, patents, and health
registrations, we have established a dedicated area to address your inquiries on these matters
and any other issues related to our operations.

Cannabis Research

CANARITECH CRO

Canaritech CRO is a leading provider of research protocols tailored to the unique requirements
of cannabis medicines.

Our Principles

Regulatory Compliance

CANARITECH is firmly committed to ensuring that all of its operations are conducted in strict
compliance with all applicable national and international regulations. Consequently, we have
established rigorous protocols and procedures to ensure compliance with Good Clinical
Practice (GCP)
.

As the development of our research protocols involves the participation of human beings,
CANARITECH adheres to an international standard of ethics and scientific quality in the design,
conduct, recording, and reporting of studies conducted by researchers assigned to the
protocols.

The rights, safety, and well-being of study subjects are protected in accordance with the
principles set forth in the Declaration of Helsinki and the resulting clinical data are credible.

¹ At CANARITECH, we comply with and require compliance with the Declaration of Helsinki in its
2013 version, as issued by the World Medical Association, as well as the Taipei Declaration on
Ethical Considerations for Health Databases and Biobanks.

About Us

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A word from

Our Founder

The Team

Francisco Kuri Breña

Founder

Alejandro Nicolás Aguirre Oviedo

Carlos Díaz Tufinio

Past Studies

Coming Soon

Let's Collaborate

Our research staff, including study coordinators, assistants, nurses, and recruiters, undergo
regular training on regulatory compliance with the provisions issued by Cofepris.

Tell Us About your Project

If you have any inquiry or need more information, please feel free to contact us. We are here to help you every step of the way.

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