Food and Drug Administration

The FDA is renowned for its work in regulating the development of new drugs. The FDA has developed rules regarding the clinical trials that must be done on all new drugs. Currently, pharmaceutical companies must test drugs through four phases of clinical trials before they can be marketed to individuals.  Resubmission of failed applications is costly, delaying marketing approval and the availability of new drugs to patients. The full economic impact analyses of significant FDA regulations are no longer published in the Federal Register but are available on this site.

  • Food Safety Moderanization Act (FSMA)
  • Arsenic in Food
  • Nano Technology
  • Pediatrics

Related Conference of Food and Drug Administration

May 11-12, 2017

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(10 Plenary Forums - 1 Event)
San Antonio, Texas, USA

Food and Drug Administration Conference Speakers

Recommended Sessions

Related Journals

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