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

October 30-November 1, 2017

3rd Annual Congress on Rare Diseases and Orphan Drugs


(10 Plenary Forums - 1 Event)
San Antonio, Texas, USA
November 06-07, 2017

3rd International Conference on Flu and Emerging Infectious Diseases

Las Vegas, Nevada, USA
December 07-08, 2017

EuroSciCon Conference on STD-AIDS

Rome, Italy
March 1-2, 2018

5th International congress on Infectious Diseases

Berlin, Germany
June 11-12, 2018

4th World Congress on Rare Diseases and Orphan Drugs

Dublin, Ireland
July 23-25, 2018

11th World Congress on Infectious Diseases and Therapy

Melbourne, Australia
August 13-14,2018

Global Experts Meeting on Infectious Diseases

Tokyo,Japan
August 27-28, 2018

9th International Conference on Emerging Infectious Diseases

Zurich, Switzerland
September 17-18, 2018

4th Annual Congress on Infectious Diseases

San Diego, USA
September 27-29, 2018

10thEuro-Global Conference on Infectious Diseases

Rome, Italy

Food and Drug Administration Conference Speakers

Recommended Sessions

Related Journals

Are you interested in