The FDA's Commissioner of Food and Drugs, Robert M. Califf, M.D., will be the Keynote Speaker.
The Office of Research Compliance and Quality Assurance in collaboration with FDA Office of Regulatory Affairs Florida District Office and the FDA Office of Minority Health is pleased to invite you to a Clinical Trial Symposium entitled: “Improving Clinical Research in the Age of Precision Medicine,” featuring Keynote Speaker Dr. Robert M. Califf, FDA Commissioner.
The event will take place on September 14 and 15, from 8 a.m. to 5 p.m., at The University of Miami BankUnited Center, 1245 Dauer Drive, Coral Gables. The cost of registration for the two-day seminar is $175.00 (breakfast, lunch and refreshments for both days are included).
The 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. CME and/or CEU’s credits will be provided to all registered participants.
Registration will close on September 9. Complete registration here. For more information, please contact Johanna Stamates at firstname.lastname@example.org or Patty Tate at email@example.com.