Beaufort CRO
Research ServicesVirginia, United States51-200 Employees
94% of our clients rate us higher than other CROs. Why? Because our partnerships with life science companies are defined by access, adaptability, and relentless accountability. Those partnerships accelerate MedTech innovations to market through agility and precision. As an agile MedTech CRO, we bring deep expertise across medical devices, in vitro diagnostics, and emerging technologies, supporting complex regulatory requirements, clinical trial execution, and data needs with clarity and discipline. AGILITY When speed matters, agility matters more. At Beaufort, agility is reflected in senior-level engagement, direct access to decision makers, and the ability to adjust strategy and execution without losing continuity or control. Our teams stay closely connected, anticipate regulatory and operational challenges early, and remain fully accountable from initial planning through submission and beyond. THERAPEUTIC EXPERTISE Our teams bring extensive experience across a wide range of therapeutic areas and medical specialties, including cardiovascular, orthopedics, neurology, oncology, women’s health, infectious disease, and digital health. We are highly experienced in diagnostics, companion diagnostics, and software-driven and AI-enabled technologies, with a strong understanding of the regulatory and clinical nuances that shape development and commercialization in these categories. The result is a CRO with a reputation built through consistently disciplined execution, thoughtful problem-solving, and trust earned through action. Our experience includes: • 20+ years of experience • 500 plus regulatory submissions including 510(k)s, PMAs, IDEs, and CE Marks• 4,000 plus clinical study sites worldwide • 1,000 plus clinical trials across diverse indications and testing platforms • 2,600 clinical professionals in more than 50 countries https://beaufortcro.com/
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support@leadiq.com 
