Beaufort’s clinical trial management services are supported by a highly qualified team of diagnostic and medical device experts. Our proven track record in managing both domestic and international clinical trials from beginning to end sets the foundation of a lineup of industry-leading services. We will fully manage and provide strategic assistance for every phase of your clinical trial. Or, we will provide one or more stand-alone services as a functional service provider to complement your internal staff.
Services We Provide Include:
- Study and protocol design and review
- Case report form (CRF) design and development
- Informed consent development and review
- Clinical investigator evaluation, qualification and selection
- Clinical or laboratory site identification, qualification and initiation
- Clinical trial management and coordination
- Selection, training and management of therapeutically qualified Clinical Research Associates (CRAs)
- Trial Master File (TMF) creation and management
- Institutional Review Board (IRB)/Ethics Committee (EC) submission support
- Medical and safety monitoring
- Conduct of investigator meetings
- Database development and management
- Statistical analysis and review
- Sample size calculations and power analysis
- Interim and final reporting
- GCP audits and training
Read case studies of how Beaufort has helped clients meet their Clinical needs.