Expertise at every stage of the development process
For 20 years, Beaufort has provided our MedTech clients with an unmatched combination of strategic insights, specialized expertise, and operational excellence to move their medical innovations forward. Learn more about our full range of services and how Beaufort’s global team can support your diagnostic and medical device development.
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Clinical Trial Services
Clinical Trial Services
Comprehensive clinical trial support from study start-up through enrollment to close out.
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Data Management
Data Management
Our data-centric approach maximizes data integrity and quality – and ensures your data is submission-ready.
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Biostatistics
Biostatistics
Strategic consulting, statistics, and statistical programming to deliver actionable insights, analyses, and reporting.
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Regulatory Affairs
Regulatory Affairs
Results-focused regulatory strategies, protocol development, and pre- and post-market submission and support.
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Companion Diagnostics
Companion Diagnostics
Seamless integration and coordination of all aspects of CDx co-development from feasibility through approval.
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Quality Assurance
Quality Assurance
QMS design and implementation, gap assessment and remediation, auditing and inspection readiness.
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