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The FDA also has to review and approve in a
timely manner the safety and efficiency of new drugs, biologics, medical devices, and
animal drugs. They have to monitor the safety and effectiveness of new medical
products after they are marketed and acting on the information collected. The FDA is
responsible for seeing that the public has access to truthful and non-misleading product
information by: monitoring the promotional activities of drug and device manufacturers,
and regulating the labeling of all packaged foods.
Science is a big part of the FDA organization. The scientific evidence needed to
back up FDAs legal cases is prepared by the agencies 2,100 scientist, including 900
chemist and 300 microbiologist, who work in 40 laboratories in the Washington, D...
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