Therapeutic expertise

In a competitive and highly regulated clinical research environment, sponsors need partners who combine global coordination with therapeutic and regulatory depth. At ABRS, we offer tailored support through two flexible service models: Functional Service Provider (FSP) and Clinical Oversight Management (COM).

These models are built around one goal: to help sponsors deliver high-quality results in complex, multiregional clinical trials—faster and more efficiently.

Scalable Support Through the FSP Model
Our FSP model allows sponsors to scale clinical trial operations without increasing permanent headcount. ABRS provides highly qualified professionals—CRAs, CTAs, regulatory leads, and more—who integrate directly into sponsor teams.

Each assignment is matched with personnel who bring both operational experience and therapeutic expertise. This ensures faster onboarding, protocol understanding, and regulatory alignment from day one.

Whether you need a single function or full study support, our Functional Service Provider approach is designed to flex with your pipeline needs.

Therapeutic Expertise That Drives Outcomes
Over the past 15 years, ABRS has supported clinical trials across diverse therapeutic areas, including oncology, infectious diseases, neurology, and rare diseases.

This therapeutic expertise gives our teams the ability to anticipate trial challenges, tailor communications with investigative sites, and support protocol-specific procedures effectively.

By combining deep therapeutic insight with process-driven FSP delivery, we strengthen both trial quality and execution.

Clinical Oversight Management (COM) for Greater Control
For sponsors working with external CROs or managing complex studies, our Clinical Oversight Management (COM) service offers structured governance and quality oversight.

COM ensures that all study activities—regardless of who executes them—remain aligned with sponsor expectations, ICH-GCP standards, and regional regulations.

We monitor key indicators, coordinate communication, and escalate risks proactively. This level of structured oversight gives sponsors greater control without increasing operational burden.

Global Clinical Trial Support with Local Precision
ABRS delivers FSP and COM services across LATAM, Europe, and Asia Pacific. We adapt execution strategies to local requirements. 

By combining global clinical trial support with local regulatory fluency, we reduce start-up delays, improve site compliance, and enhance data quality.

This geographic adaptability is essential in multiregional trials, where timelines and regulations vary widely.

Integration with Sponsor Teams and Systems
Our FSP professionals are trained to work within sponsor SOPs and platforms. They are not just vendors—they are embedded partners.

In our COM model, ABRS establishes oversight mechanisms that align with sponsor governance structures. This ensures consistent reporting, better issue resolution, and full traceability across vendors and regions.

By integrating tightly with sponsor workflows, we reduce friction and increase transparency.