Sponsor Section
What We Do
Phase I-IIA Confined Short and Long Term Studies
- First entry into mankind studies in all therapeutic sub-specialties
Research Support Services
- Solicitation of Clinical Trials
- Identification and recruitment of principal investigators
- Protocol development and study design
- Protocol and informed consent review by Western Institutional Review Board (WIRB)
- Budget preparation and execution of contracts between sponsors and the university
- Experienced staff to conduct clinical trials
- Patient recruitment and monitoring
- Data collection and data management
- Continuous personnel training (CCRC)
- Post-study report and manuscript preparation
- Central data coordinating center
- Biostatistical support
- Analytical toxicology core laboratory support
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Diverse Therapeutic Areas/Studies
- Antiarrhythmic Cardiac Drugs
- Radioactive Labeled Compounds
- Antifungals
- Antivirals
- Age Gender Studies
- QTC Prolongation Studies
- Renal Impairment Studies
- ADME Studies
- Mass Balance Studies
- Drug/Drug Interaction Studies
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Diversified Patient Database
- Healthy Adult Populations
- Special Populations
- Elderly
- Diabetic
- Obese
- Post Menopausal
- Compromised Populations
- Hepatic Insufficiency
- Renal Insufficiency
- Cardiac Insufficiency
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©2005 University of Florida | Center for Clinical Trials Research Phase I. All Rights Reserved.
2401 SW Archer Rd.
Gainesville, FL 32608
Email Us: thomprd@ufl.edu
Call Us: 352.273.5500
Fax: 352.273.5541