Toll-free: +1 888 745 2727  – Email: [email protected]

BRCR CRO

Ready to Boost Clinical Trial Development?

 Toll-free: +1 888 745 2727 – Email: [email protected]

Profit from new markets

The United States, Latin America and the Caribbean are considered good regions for the development of Clinical Trials, and we are here to help you enter the market.

The benefits

Highly Qualified Medical Professionals

Through our network of sites and doctors, we ensure that we have only the best doctors in the various medical specialties, with extensive knowledge in the area of research, health care and patient relations.

Great diversity of patients

Latin America has a population of approximately 600 million people, many of whom live in areas where state health services are saturated, so recruitment efforts can be optimized, radically improving health development.

Low competition for patients

Compared to the USA and EU, Sponsors and CRO competition for patients in Latin America is low. LATAM has a higher Patient-Compliance, and thanks to the high concentration of potential subjects, fewer sites will be required to conduct the study.

BRCR Latam

FDA FACT:
“Ensuring diversity in clinical trials is key to advancing health equity”

We are constantly expanding our network of sites, researchers, teams, to better serve sponsors and patients. We have a strong pressence in LATAM, serving Mexico, Ecuador, Puerto Rico, Guatemala, El Salvador, Honduras, Costa Rica, Panama, Peru, Brazil, Paraguay, Jamaica, and Dominican Republic.

Why Work With Us?

Site Selection

Through our feasibility studies, we can determine the sites where the development of the clinical trial will be most profitable for the sponsor, based on the type of study, the number of patients to meet enrollment targets, and the time frame needed for its development.

Optimized Proccess

Our goal is to save time for the Sponsor, so over the years, we have refined our processes to optimize them as much as possible. This allows us to streamline regulatory procedures, patient recruitment, and quality assurance to ensure the smooth running of the clinical trial.

Regulatory & Legal Affairs

Our regulatory team has the knowledge and expertise necessary to ensure compliance with the requirements of the various authorities that regulate clinical research activities in the different countries of Latin America.

Recruitment and Retention

Thanks to the large pool of potential patients, patient recruitment and retention activities are highly favored in Latin America. Through various recruitment strategies, we are able to achieve our goal in a short time frame.

Full study management

You can leave all the study management in our hands. Our main service as CRO is the management of clinical studies, from Start-up to Closure, regardless of the phase of the study, our team of experts is trained to handle the project quickly and efficiently.

Ready for The Americas?