Clinical studies, clinical evaluations
Capabilities...
- Outcomes and "me too" based clinical studies
- Complete clinical research management
- Develop investigational protocols
- Develop informed consent forms
- Develop case report forms Download a sample CRF
- Obtain IRB approval
- Luminary site setup, education, and clinical study roll-out
- Investigational protocol change management
- Audits and monitoring
- Recordkeeping audits
- Annual reviews
- Clinical study closure
- Data integrity management
- Web-based data capture and data binning
Track record...
- Over 100 devices documented in clinical investigational protocols and IRB-approved
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