Expertise to Conduct Clinical Trials

Clinical Trials in: Mexico, Argentina, Colombia and Brazil.

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As a leading CRO in LATAM, we specialize in supporting clinical trials throughout the region. Our extensive experience and broad network of clinical sites enable us to execute trials with speed and efficiency, ensuring high patient recruitment and retention rates.

Expertise to Conduct Clinical Trials in Argentina

Expertise to Conduct Clinical Trials in Argentina – Clinical Trials in Latin America

Clinical trials serve as the backbone of medical progress, propelling scientific breakthroughs and revolutionizing patient care. In recent years, Argentina has emerged as a thriving hub for clinical research, offering a blend of diverse patient populations, well-established medical infrastructure, and a conducive regulatory environment.

Yet, the key to unlocking the full potential of clinical trials in Argentina lies in the expertise required to navigate its intricacies. This blog delves into the expertise necessary to conduct successful clinical trials in Argentina, shedding light on the opportunities, challenges, and insights that researchers and organizations can harness.

Unveiling Argentina’s Clinical Trial Landscape:

  1. Diversity in Patient Demographics: Argentina’s populace represents a mosaic of ethnicities, ages, and medical backgrounds. This diversity provides a unique opportunity to conduct trials with a wide-ranging patient pool, enhancing the applicability of research outcomes.
  2. Advanced Medical Infrastructure: Major cities in Argentina boast state-of-the-art medical facilities and research centers, laying a solid foundation for conducting trials across various therapeutic domains.
  3. Cost-Efficiency: Conducting clinical trials in Argentina often proves cost-effective, appealing to sponsors and researchers aiming to optimize budgets without compromising the quality of their studies.
  4. Regulatory Environment: Argentina has taken substantial strides in establishing a robust regulatory framework for clinical trials, adhering to international standards and ethical guidelines. This framework fosters consistency and ethical conduct throughout the research process.

Essential Expertise for Success:

  1. Regulatory Navigation: Navigating Argentina’s regulatory landscape is pivotal. Researchers and sponsors must possess an in-depth understanding of regulatory procedures and secure approvals from the National Administration of Drugs, Food, and Medical Technology (ANMAT).
  2. Ethical Prowess: Upholding ethical standards is paramount. Professionals conducting trials in Argentina must adhere rigorously to globally recognized ethical norms, safeguarding the rights and well-being of study participants.
  3. Local Collaboration: Collaborating with local investigators, healthcare professionals, and site staff is integral. Local experts offer valuable insights into patient demographics, cultural nuances, and healthcare practices that shape trial design and implementation.

Effective Communication: Effective communication bridges gaps in collaboration. While English is widely used, proficiency in Spanish—the official language of Argentina—or employing bilingual staff ensures seamless interactions during trial conduct.

Expertise to Conduct Clinical Trials in Argentina

Expertise to Conduct Clinical Trials in Argentina

Expertise to Conduct Clinical Trials in Argentina

Overcoming Challenges:

  1. Language Barrier: Despite English being prevalent in professional settings, language barriers can still arise. Bilingual staff or professional translators can facilitate effective communication and understanding.
  2. Logistical Complexities: Argentina’s geographical vastness can present logistical challenges, particularly in multi-center trials. Meticulous planning and coordination are vital to ensuring smooth data collection and reporting.
  3. Cultural Considerations: Cultural variations influence patient engagement, recruitment, and retention. Customizing recruitment strategies to align with local customs can enhance patient involvement.
  4. Data Integrity: Ensuring data accuracy and quality control across diverse sites requires standardized training and vigilant monitoring. Regular site visits and remote oversight play pivotal roles in upholding data integrity.

Sustaining Success:

To sustain the trajectory of clinical trials in Argentina, ongoing education about regulatory changes, best practices, and ethical conduct is vital. Staying informed and sharing insights with peers contribute to the long-term success of clinical research in the country.

In Conclusion:

Argentina’s ascendancy as a clinical trial destination is a testament to its potential to contribute to global medical advancements. The synergy of diverse patient populations, advanced medical infrastructure, and cost-effectiveness creates a compelling proposition for researchers and sponsors.

However, realizing this potential hinges on the mastery of expertise required to navigate regulatory intricacies, uphold ethical standards, and collaborate effectively with local professionals. As Argentina continues to shape the medical research landscape, maintaining elevated standards of expertise and ethical conduct will cement its pivotal role in the global clinical trial arena.

Through the harmonious interplay of these elements, Argentina stands poised to not only expand scientific knowledge but also elevate patient care on a global scale.

Expertise to Conduct Clinical Trials in Argentina

Source: World Courier

Welcome to Cohortias!

of Latin America

Simplify Your Clinical Trials with Our Expert Infrastructure in Latin America

Say goodbye to the complex, costly, and disorganized process of conducting clinical trials. Our infrastructure in Latin America streamlines the launch of studies and ensures adherence to international standards. Schedule a call with us today to discover the path to simplified clinical research in Latin America.

Expertise to Conduct Clinical Trials

Explore What We Are Doing Better

We define ourselves as a unique team, capable of blending our academic background with a global business mindset to bring the highest standard of quality and operational excellence into clinical research in Latin America.

Early Phase Trials

- First-in-Human Studies.
- Get to patients faster, no IND necessary.
- Valid data for FDA submission.

Rescue Studies

- Regain lost time and boost patient recruitment.
- We work alongside Global CROs to get studies back on track.
- More than 200 sites available.

Phase II & III Trials

- Full-Service Clinical Outsourcing.
- Proven infrastructure that can handle any trial.
- Local Regulatory Experts
- Wide network of sites and physicians.

Medical Devices

- A fast-track platform that will meet your timeline.
- We take care of everything, from shipping requirements all the way to data collection.
Expertise to Conduct Clinical Trials

Full Service CRO in LATAM

Outsourcing Clinical Trials to Latin America

Unlock the advantages and opportunities of outsourcing clinical trials to Latin America. Diverse patient population, streamlined regulations, and cost-effectiveness

Lower Operating Costs

From lower labor costs to lower costs for rent, utilities, and equipment, you can save money on your clinical trial budget while still ensuring the quality of your trial

Access to Emerging Markets

Latin America offers access to emerging markets, providing an opportunity for pharmaceutical companies to expand their reach and reach new patient populations.

Expertise to Conduct Clinical Trials

Cohortias is redefining Clinical Research in Latin America

We are committed to become leaders in providing clinical research services in Latin America. Here at Cohortias, we combine our academic roots, proven experience and a large pool of patients from an extensive network of sites.

Our main purpose is to deliver high quality data.

Expertise to Conduct Clinical Trials

Clinical Research in Latin America

Cohortias has built an extensive and highly reputable network of clinical sites which can access patients in a timely manner and operate within a standard-of-care comparable to the U.S. healthcare system.


  • Site Management

  • Data Management

  • Site Selection

  • Regulatory Submissions

  • Clinical Monitoring

  • Protocol Development


Beta Trials Platform

  • First-in-human studies

Medical Devices

  • Pilot and Pivotal Device Studies

Phases I – III

  • We partner with our clients to bring their products in a fast and efficient manner to the market with the highest quality standards


  • Diabetes/Metabolic Syndromes
  • Infectious Diseases
  • Cardiovascular
  • Neurology
  • Respiratory
  • Oncology

Expertise to Conduct Clinical Trials

Clinical Research in Latin America

Academic Leadership and Extensive Clinical Site Network for Efficient Clinical Trials

  • Our peer-to-peer management approach guarantees high patient recruitment and retention in any clinical trial

High Speed Execution

  • We offer the quickest start-up times in each country.
  • Efficient Clinical Site Selection and Contracting.
  • Benefit from our extensive network of clinical sites and streamlined contracting process.

Operational Excellence

  • Proven record of delivering rescue studies, we consistently exceed industry performance standards.
  • Our team provides efficient query resolution to keep your trial on track.

Business Insight and Flexibility

  • We offer innovative pricing models and short lines of communication to ensure maximum flexibility and cost-effectiveness.
  • At Cohortias, we prioritize  short lines of communication to ensure efficient collaboration.
  • Swift adaptation to changes in the trial landscape to keep your study on schedule.

Expertise to Conduct Clinical Trials

We provide our services with offices in:

Colombia &

Daniela Maresca
Daniela Maresca | Country Lead Argentina
Martín Hernández-Torre | CMO
Maritza Rojas | CRA II
Pedro Alvarez | Business Development Manager
Samantha Rodriguez Cohortias
Samantha Rdz. | Start-Up Manager
Expertise to Conduct Clinical Trials

The Cohortias Team

Expertise to Conduct Clinical Trials

As the largest South American Contract research Organization, we know the Advantages and Challenges Of the Region

Let Us Guide You Through The Latin American Clinical Research Landscape

Expertise to Conduct Clinical Trials

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