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.
We understand medical device regulation and the design and conduct of device clinical trials.
Our clinical research services for medical device 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 and adverse event reporting
- Investigator meetings
- Data management strategy
- Database development and management
- 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 medical device manufacturers.
