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This essential course offers an ethical framework for human subjects regulations, introduces regulatory issues in clinical trials, and reviews concern for human subjects protection in drug/device trials. A mock IRB meeting applies the principles learned.

Other Credits : BRN: 16 CE hours.

  • NOTE  Required course in Professional Certificate program. Prerequisite: FPM 40173, The Drug Development Process.

  • COURSE NUMBER  FPM-40388
  • CREDIT  2.00 unit(s)


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