Clinical Research
At Beaufort, we are committed to helping our clients accelerate medical innovation by delivering well-designed solutions that are tailor-made to our clients’ particular needs and circumstances. To this end, we can take full responsibility for a clinical study - from protocol design through submission of the study report - or we can provide one or more stand-alone services to complement your internal and other resources.
Our clinical research services for biopharmaceutical and biologics companies include:
- Study and protocol design
- Case report form (CRF) design and development
- Clinical site/investigator evaluation, qualification, and selection
- Study management and coordination
- Trial initiation and clinical monitoring
- Medical/safety monitoring
- Investigator meetings
- Data management strategy
- Database development and management
- Medical coding, data entry, and quality control
- Statistical analysis and review
- Interim and final reporting
- cGCP audits and training
Review case studies regarding Beaufort’s clinical research services for biopharma and biologics companies.
