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Use Cases
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Resources
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Pricing
1862
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TH e FDA is the Food an d Drug administration. It is the oldest consumer protection agency.
1906
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The first major legislation which was lead by Harvey Wiley. He researched the effects of chemical preservative used in food and drugs
1912
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The Wiley Act resigned from the FDA who decided to focus on drug regulation
1912
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The Supreme court decided that that the law of enforcing the regulation of drugs did not apply to false therapeutic claims. The supreme court ruling undermined the Wiley Act.
1927
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The FDA's name was changed to the Food, Drug, and Insecticide Administration in 1927
1930
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The name of the FDA was shortened to the Food and Drug Administration which is its name sake currently
1933
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The FDA was able to change its scope to focus on quality and standards for food and drugs, prohibition of false therapeutic claims form drugs and coverage for cosmetics and medical devices
1938
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An act that made is a requirement for companies to prove their products we FDA tested before putting them on the market
1951
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Clarified what was a prescription drug versus what was an over the counter drug
1953
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1962
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The Act was enacted to ensure the safety and effectiveness of medications of the U.S market
1965
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It monitored the use and abuse of amphetamines, barbiturates and other potentially addictive agents but this act was eventually delegated to the DEA
1968
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1976
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Allowed the FDA to approve and regulate medical devices and to recall ineffective or dangerous medical devices
1980
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The department of health was newly created
1983
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This act targeted rare diseases. It expanded research and availability of new treatments for AIDS, cancer, and genetic diseases