Clinical Research Services LATAM
Clinical Trials Supported
Participating Patients
Satisfied Clients
Clinical Research Services LATAM with 300+ Professionals Supporting Global Sponsors
Clinical Research Services LATAM by ABRS provides sponsors with access to a powerful network of 300+ dedicated professionals across the region. Latin America has become one of the fastest-growing hubs for clinical trials, offering sponsors unique opportunities such as diverse patient populations, accelerated recruitment, and cost-effective study execution. At ABRS, we harness this potential by delivering end-to-end services: feasibility assessments, regulatory submissions, patient recruitment, trial monitoring, and study closeout. Our multidisciplinary team ensures that every study is conducted in full alignment with FDA, EMA, and ICH-GCP standards.
Managing trials in LATAM can present challenges such as regulatory variations, cultural diversity, and logistical complexity. With our Clinical Research Service LATAM, sponsors gain direct access to experienced project managers, clinical research associates, regulatory specialists, and data experts who anticipate these challenges and deliver proactive solutions. Our 300+ professionals bring both local knowledge and international expertise, ensuring seamless integration of regional operations into global programs. This capability reduces risks, accelerates timelines, and guarantees that studies are audit-ready at all times.
Trusted Clinical Research Service LATAM Backed by 300+ Professionals
Clinical Research Services LATAM at ABRS goes beyond operational support—it is a strategic solution built on trust, precision, and measurable value. With 300+ professionals dedicated to clinical research across LATAM, we provide sponsors with the scale and expertise to manage complex studies in multiple countries simultaneously. Our services include vendor oversight, regulatory compliance checks, quality assurance, and performance monitoring, ensuring consistent standards and transparency throughout the study lifecycle.
Technology plays a central role in our oversight model. ABRS integrates digital platforms that streamline reporting, automate workflows, and provide real-time visibility into study milestones. This enables sponsors to make faster, data-driven decisions and ensures that collaboration between CROs, sites, and global teams remains efficient. Our experts also maintain close relationships with regulatory agencies and ethics committees in the region, facilitating faster approvals and reducing bottlenecks.
By partnering with ABRS for Clinical Research Service LATAM, sponsors gain a trusted regional ally capable of transforming LATAM’s potential into reliable outcomes. Our 300+ professionals combine local insight with global standards, safeguarding patient safety, ensuring data integrity, and accelerating trial success. Ultimately, ABRS transforms the complexity of conducting clinical research in Latin America into an opportunity for sponsors to expand their global footprint with confidence, compliance, and operational excellence.
Study Design
Regulatory Submissions
Site Selection
Data Management
Successful Execution of Clinical Trials
End-to-End Trial Management
2. Ethical and Regulatory Compliance:
• Our team is committed to upholding the highest ethical standards and ensuring strict adherence to regulatory requirements in LATAM. Trust us to navigate the complex landscape and keep your trials in compliance.
3. Strategic Protocol Development:
• Benefit from our experience crafting strategic and effective study protocols tailored to the specific requirements of your research objectives, ensuring clarity and precision.
4. Patient Recruitment and Retention:
• We employ targeted strategies to recruit and retain study participants efficiently, optimizing timelines and contributing to the overall success of your trials.
5. Quality Assurance and Monitoring:
• Rigorous quality assurance measures and proactive monitoring protocols are implemented to uphold the integrity of your data and ensure the reliability of study outcomes.
6. Specialized Expertise:
• Our team consists of seasoned professionals with specialized expertise in diverse therapeutic areas, providing valuable insights to enhance the quality and relevance of your medical research.
7. Customized Solutions:
• Recognizing the unique nature of each clinical trial, we offer flexible and customized solutions that align with your specific goals and budget constraints.
Why Choose Clinical Research Services LATAM:
FAQ's
ABRS offers a comprehensive range of services, spanning from study start-up to close-out, covering various phases of clinical research. This includes support for first-in-human trials, dose-ranging studies and pivotal trials.
ABRS provides critical insight, support, and best practices to ensure the success of clinical trials. Our commitment is to offer solutions that empower you to innovate with confidence, seize opportunities, and propel your clinical trials forward.
ABRS distinguishes itself by offering a broad spectrum of services that covers the entire clinical research process. We go beyond traditional support, providing not just services but also critical insights to help our clients navigate challenges and make informed decisions.
ABRS is dedicated to facilitating innovation in clinical research. We not only provide support for various phases of research but also aim to enhance opportunities for our clients. Our goal is to drive clinical trials forward by ensuring that our clients can navigate the complexities of the process with confidence.
ABRS has extensive experience in conducting clinical research in fourteen countries. Our global reach allows us to navigate diverse regulatory environments, ensuring seamless and compliant clinical trials.
ABRS boasts a highly skilled and experienced professional team dedicated to clinical research excellence. Our team members bring diverse backgrounds and expertise, collectively contributing to successful outcomes across various phases of clinical trials. With years of experience, they navigate complexities, providing clients with the confidence to overcome challenges in the ever-evolving landscape of clinical research.
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