Clinical Trial Capabilities
CEDRA Clinical Research, LLC offers investigational site research services for Phase I-IV clinical trials. We provide a unique brand of experience, personalized research services and flexibility, which keep our clients coming back. Tight timelines, difficult enrollment qualifications and unusual study guidelines are challenges our staff welcomes.
Strong Teams
CEDRA Clinical Research's Medical Director and our experienced team of clinical investigators have conducted over 600 studies with more than 14,000 subjects in various therapeutic areas and models of clinical investigation. Our medical personnel have served as principal investigators in numerous pivotal studies.
Day-to-day oversight by experienced study coordinators provides continuity from start to finish. Our coordinators are involved in every aspect of a study, including patient recruitment, source document development, resource allocation and coordination, and patient data collection through various paper-based and electronic data capture technologies.
CEDRA Clinical Research's experienced Phase I/Bioequivalence team offers protocol and CRF design as well as data management and study report preparation services.
Performance Efficiencies
Remote data entry, computer generated source documents, expanded data base with multiple therapeutic categories and special populations.
Clinical Trial Experience
- Allergy
- Dermatology
- Diabetes
- Gastritis
- Hypertension
- Migraine
- Opthalmology
- Pain Management
- Phase I
- Quality of Life
- Women's Health Studies
Enhanced Facility Capabilities
- Centralized clock system
- Fully equipped sample processing laboratory
- Security alarmed -70°C freezer
- Limited-access Phase I unit
- Federal and State Schedule II-IV drug licensure
- Spacious procedure areas
- Full-service clinical laboratory
