Presenting the FDA/University of Miami Conference: Improving Clinical Research in the Age of Precision Medicine – Clinical Trials Symposium
This symposium will focus on scientific, regulatory, and ethical aspects of clinical
trials as well as quality assurance practices. It will provide important updates on
FDA regulatory requirements for clinical trials and perspectives from the front
lines of clinical research.
When: Sept 14-15, 2016
Where: The University of Miami | Bank United Center | 1245 Dauer Drive, Coral Gables, FL 33146
Keynote Speaker: Dr. Robert Califf, Commissioner, U.S. FDA
Topics include:
Compliance in Clinical Research
Regulatory Perspective: Recruitment Challenges
Understanding the Principal Investigator’s Responsibilities
CME and CEU credits available. For more information, please contact:
Johanna Stamates at jstamates@med.miami.edu or Patty Tate at plt18@miami.edu.
Presented by:
The University of Miami Office of Research Compliance and Quality Assurance in collaboration with the FDA Office of Regulatory Affairs Florida District Office and the FDA Office of Minority Health.
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