Our Commitment to Quality Results
At CEDRA we provide complete services relating to early phase drug development. Our clinical expertise ranges from assistance with initial study design all the way to preparation and submission of final reports. CEDRA’s modern clinical research and development sites in Austin and San Antonio, Texas, are GCP/ICH compliant, with all the essential facilities for storing and dispensing study drugs, along with maintaining regulatory documents and study data. Specimens are seamlessly transferred to our bioanalytical services division for sample analysis.
At CEDRA, our commitment to your success means we’ve developed a team of dedicated individuals with significant experience in a broad range of therapeutic areas and kept their skills up to date with a program of ongoing training and continuing education. Our high retention rate of key employees has allowed us to cultivate exceptionally strong teamwork over the years, providing consistency and continuity that benefit you and your studies.
Therapeutic Experience (Added experience through relationship with WCT)
- Allergy
- Alzheimer’s disease
- Anxiety disorders
- Bipolar disorder
- Cardiovascular disease
- Depression
- Diabetes
- Hypertension
- Mild cognitive impairment
- Ophthalmology
- Pain models and management
- Parkinson’s disease
- Women's health studies
Facility Capabilities
- Centralized atomic clock system
- Class 10,000 clean room
- Federal and State Schedule I-V (Austin), II-V (San Antonio)
- Fully equipped sample processing laboratory
- Full-service clinical laboratory
- Limited-access Phase I unit
- Radiolabel licensure (Austin)
- Serial and continuous CSF equipment
- Security alarmed -70˚C and -20°C freezers
- Spacious procedure areas
- Telemetry equipment