Global FSP Partner for Clinical Oversight and Trial Execution
About Us
At ABRS, our dedication to success goes beyond borders, reaching across different parts of the world. With extensive experience in various regions, we offer unmatched expertise in organizing and overseeing clinical trials using our tailored Functional Service Provider (FSP) Models. This method ensures the provision of practical know-how, scalability, and efficient resource management for our clients’ clinical trials in North America, Latin America, Europe, and Asia-Pacific.
A team of experts familiar with regional rules and cultural differences strengthens our global presence. This comprehensive understanding enables us to navigate the complexities of diverse areas, ensuring the success of your clinical trials with ABRS. Join forces with us for a genuinely global and successful clinical trial experience.
Benefits of Our Tailored and Scalable FullSpectrum FSP Model
Goals
Services are completely scalable
Only pay for what you use
Resources
Communications
We report directly to you
Process Stability
Decentralized monitoring and subject visits
Qualified Staff
High-level certified FSPs
Project Control
The work is performed per your SOPs and using your systems
Tailored Functional Service Provider
Discover the difference with ABRS Tailored FSP – your customized solution for clinical research success ...
Traditional Services
ABRS provide various Traditional Services such as Safety and Pharmacovigilance expertise, Study Start-Up, Biometrics ...
Let's Explore
ABRS delivers flexible Functional Service Provider (FSP) and Clinical Oversight Management (COM) services across all phases of clinical research—from start-up to close-out.
Our expert teams integrate operational support, regulatory insight, and therapeutic expertise to deliver tailored, high-impact solutions.
This cohesive approach streamlines processes, reduces risk, and improves trial performance across global regions.
We align our FSP and COM strategies with each project’s evolving needs—ensuring quality, compliance, and speed from day one.
Through open communication and proactive oversight, we help sponsors navigate complexity with confidence and control.
Whether optimizing local studies or managing global operations, ABRS brings clarity, consistency, and measurable value at every stage of your clinical development journey.
Non-Traditional Services
ABRS provide various Traditional Services such as Trial Master File (TMF), Clinical Trial Disclosure, Regulatory, Administrative ...
Clinical Oversight Management (COM)
Clinical Oversight Management (COM) is a comprehensive service designed to provide ...
Clinical Research Services LATAM
Embark on your clinical trials with confidence through our specialized Clinical Research Services ...
We utilize our resources to help you
Address problems efficiently and effectively
Manage Documents effortlessly
Standardize Workflow
Safety and Quality
We utilize our resources to help you
Address problems efficiently and effectively
Manage Documents effortlessly
Standardize Workflow
Safety and Quality
Our Impact
FAQ
Clinical Research Solutions Ask, Discover, & Understand
ABRS offers a comprehensive range of services, spanning from study start-up to close-out, and effectively covering all key phases of clinical research. In particular, this includes expert support for first-in-human trials, dose-ranging studies, and pivotal trials. Furthermore, our flexible and scalable approach allows us to adapt to the unique demands of each project. As a result, we ensure quality, compliance, and operational efficiency at every step. In other words, we tailor our services to match your goals while maintaining the highest standards throughout the entire clinical development process.
ABRS provides critical insight, operational support, and proven best practices to ensure the success of your clinical trials. In addition, we are fully committed to delivering solutions that empower you to innovate with confidence, seize new opportunities, and effectively propel your research forward. Moreover, by combining expertise with flexibility, we help sponsors navigate challenges and accelerate development timelines across all phases of the clinical process. As a result, our partners benefit from enhanced efficiency, reduced risk, and greater strategic alignment. Ultimately, ABRS stands as a dependable ally in driving meaningful outcomes throughout your research journey.
ABRS distinguishes itself by offering a broad spectrum of services that covers the entire clinical research process from start to finish. In fact, our comprehensive approach ensures consistent support across all trial phases. Furthermore, we go beyond traditional support by delivering not only high-quality services but also critical insights that empower our clients to navigate challenges effectively. Because of this, sponsors can make informed decisions that align with their strategic goals. As a result, we enable better decision-making, increased efficiency, and stronger outcomes throughout every stage of the clinical trial lifecycle. In summary, ABRS combines depth of expertise with a proactive mindset to deliver real value at every step.
ABRS is dedicated to facilitating innovation in clinical research through expert guidance and tailored support. To begin with, we provide assistance across multiple phases of the research process, ensuring continuity and consistency. Not only that, but we also strive to enhance opportunities for our clients at every stage, adapting our approach to meet specific project needs. Moreover, our primary goal is to drive clinical trials forward by ensuring that sponsors can navigate complex regulatory and operational challenges with clarity and confidence. As a consequence, our clients experience smoother execution, faster timelines, and improved outcomes. In the end, we help transform innovation into measurable progress that delivers lasting impact.
ABRS has extensive experience in conducting clinical research in fourteen countries. In addition, our global reach allows us to navigate diverse regulatory environments with precision and agility. Therefore, we ensure seamless and compliant clinical trials across regions. As a result, sponsors benefit from faster approvals, reduced risks, and consistent execution. In short, our international expertise translates into more efficient and successful research outcomes.
ABRS boasts a highly skilled and experienced professional team dedicated to clinical research excellence. To begin with, our team members bring diverse backgrounds and expertise, which collectively contribute to successful outcomes across various phases of clinical trials. Furthermore, this multidisciplinary approach enhances adaptability and strengthens execution. In addition, with years of hands-on experience, they navigate operational and regulatory complexities with ease. Because of this, our clients receive expert support at every critical stage. As a result, they gain the confidence needed to overcome challenges in the ever-evolving landscape of clinical research. In summary, our people are the foundation of the reliability and success ABRS delivers.
Our Latest Articles
By applying innovative thinking, we deliver intelligent solutions that empower sponsors and their study sites to disentangle the chaos of clinical trial management. Complex processes become more manageable and efficient. In turn, this enables teams to focus on strategic goals rather than administrative burden. Ultimately, our approach transforms challenges into opportunities for progress.
Our Location
At ABRS, we currently provide coverage in
North America
.
Latin America
.
Europe
.
Asia-pacific
.
Who are we
- We Offer Tailored and Scalable FSP models
- We provide COM Services to ensure ESP compliance
Patient Safety
Data Quality
Adherence to Protocols