Biometrics
Clinical Trials Supported
Participating Patients
Satisfied Clients
Clinical Research Solutions That Drive Excellence
Clinical research solutions at ABRS are built to support sponsors across the entire clinical development lifecycle, from early-phase first-in-human trials to complex late-phase studies and post-market surveillance. We combine global expertise with local regulatory insight to ensure that every study is conducted with precision, efficiency, and compliance. Unlike traditional outsourcing models, our approach as a Functional Service Provider (FSP) enables sponsors to expand internal capabilities with specialized, dedicated teams that integrate seamlessly into sponsor systems while maintaining ABRS’s commitment to operational excellence.
At ABRS, we understand that the success of clinical development depends on more than just execution—it requires foresight, adaptability, and compliance. Our clinical research solutions are designed to address these needs through strategic planning, operational efficiency, and regulatory alignment. We provide sponsors with critical insights, unwavering support, and industry best practices so that clinical trials are not only successful but also conducted with full confidence. This commitment ensures adherence to FDA, EMA, and ICH-GCP guidelines, reinforcing the highest ethical and operational standards throughout every phase.
Clinical research solutions at ABRS also prioritize transparency and collaboration. By leveraging advanced project management tools, data-driven oversight, and proactive communication, we ensure that sponsors maintain visibility and control over study progress at all times. Our global team delivers harmonized processes while adapting to local market requirements, minimizing delays and enhancing the quality of outcomes. Whether managing a single-site trial or coordinating a complex, multi-country program, ABRS delivers end-to-end clinical research solutions that adapt to the scale and complexity of each project.
Biometrics as Part of Our Clinical Research Solutions
Clinical research solutions at ABRS are strengthened by our dedicated Biometrics services, which integrate expert Data Management, Biostatistics, and Programming into every clinical trial. Our biometrics team ensures robust data handling, precise statistical analysis, and reliable programming support, enabling sponsors to make informed decisions at every stage of development. From database design to statistical reporting, we align biometrics seamlessly with trial objectives, ensuring that data integrity and accuracy are never compromised.
Our clinical research solutions leverage biometrics to accelerate timelines and reduce risks. Advanced statistical methodologies and validated programming tools provide accurate insights into patient safety, treatment efficacy, and overall study performance. These capabilities allow sponsors to optimize decision-making, meet regulatory expectations, and maintain confidence in their clinical trial data. By embedding biometrics into a comprehensive FSP framework, ABRS ensures that sponsors benefit from both operational efficiency and scientific rigor.
Clinical research solutions at ABRS also extend to COM (Clinical Operations Management), integrating site management, monitoring, and quality oversight into the biometrics and FSP model. This holistic approach ensures that study operations, safety reporting, and data analysis are fully aligned, delivering a unified strategy that drives both efficiency and quality. By combining biometrics with COM, ABRS creates synergies that accelerate trial execution while maintaining strict adherence to global regulatory requirements.
Ultimately, ABRS’s clinical research solutions provide sponsors with the assurance that their clinical trials are supported by a trusted global partner. By aligning biometrics, FSP services, and COM expertise, we deliver tailored, scalable, and high-quality solutions that adapt to every study’s unique needs. Whether advancing a single product or managing a portfolio of international programs, sponsors can rely on ABRS to provide comprehensive clinical research solutions that protect patients, ensure compliance, and accelerate innovation in healthcare worldwide.
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.
Our Location
At ABRS, we currently provide coverage in
North America
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Latin America
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Europe
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Asia-pacific
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