We understand your need to reduce time to market for your medical products. We know that lost time is lost opportunity, and that cutting corners is never an option. Knowledge and experience are the essential tools you need for obtaining product approval in today’s regulatory environment.

Beaufort Advisors combines extensive knowledge of clinical requirements and deep experience with clinical processes to help you efficiently plan, manage, and execute your clinical trials. And, our technical experts will help manage and conduct the data analysis and statistical reporting of clinical findings. Our comprehensive clinical service offerings will help you accelerate the time from research to market.

Clinical Trial Management Services
»	Study design and protocol development
»	Case Report Form (CRF) design and development
»	Clinical site evaluation, qualification and selection
»	Study management and coordination
»	Trial initiation and monitoring
»	Database development and management
»	Data entry and quality control
»	Statistical analysis and review
»	Interim and final reporting
»	Clinical procedures development
»	Good Clinical Practices (cGCP) audits and training

To discuss how Beaufort Advisors can help you achieve your clinical research and regulatory compliance objectives, please contact us at info@beaufortadvisors.com or call 757.383.6000 .