Pharma IQ Glossary: Food and Drug Administration (FDA)
Food and Drug Administration (FDA) is an agency of the United States Department of Health and Human Services. The FDA is one of the United States federal executive departments, responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), veterinary products, and cosmetics.
The Rise in New Drug Approvals in 2011
August 18 by Pharma IQThis year has already seen the number of new drugs approved by the United States Food and Drug Administration (FDA) match the total number approved in 2010. A new report compiled by Burrill & Com...
FDA Compliance: Minimising Risk
November 18 by Pharma IQCompliance with Food and Drugs Administration (FDA) guidelines is essential for all working within the pharmaceutical industry, from researchers working on clinical trials to those marketing the drugs...
FDA Guidelines
September 19 by Pharma IQ
The pharmaceutical industry in the United States has to comply with a number of guidelines to ensure the quality of the products it manufactures, the safety of its workers and members of the public, a...
