Beaufort is a global CRO built around one purpose — helping life science companies improve and save lives through the rapid development and commercialization of innovative products. Our shared interest and commitment to your success drives our entire organization to deliver best-in-class clinical trial services, regulatory strategy and planning, data and business analytics, data management and statistics, and quality services.

We are:

◈ MedTech Focused - Industry-leading expertise to streamline your clinical development.
◈ IVD Specialists - Two decades of extensive diagnostic experience.
◈ Results Oriented - Guided by efficient and adaptive clinical trial management. 
◈ Partnership Driven - 94% of clients rate Beaufort higher than other CROs

Our experience includes:

◈ 500+ Regulatory Submissions including 510(k)s, PMAs, IDEs and CE-Marks
◈ 4,000+ Clinical Study Sites Around the Globe
◈ 1,000+ Clinical Trials Across a Wide Variety of Indications and Testing Platforms
◈ 2,600+ Clinical Professionals in Over 50 Countries

See how Beaufort CRO can accelerate your medical innovation -- and put our experience to work for you.

Clinical Trials

Life Sciences

Medical Devices

Beaufort CRO

Beaufort CRO's headquarters in Virginia Beach, VA, United States

The Chicago office likely focuses on clinical trials and project management in the healthcare research sector.

Chicago

The San Diego office focuses on global regulatory affairs and quality assurance in the biotechnology and pharmaceutical sectors.

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Other offices