UF | Center For Clinical Trials Research

Sponsor Section


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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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Areas of Specialties


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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Volunteers


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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  • UF Research Resources

  • 48-Bed Phase I Study Unit
  • Clinical and basic science faculty with extensive research experience
  • Large, active clinical trials program





Visit Us
University of Florida
UF Health Science Center

©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