General History
Important Figures
Major Laws
Random Facts
Important Dates
100

This is the oldest comprehensive consumer protection agency in the United States Government. This agency inherited the 1848 chemical analysis that monitored safety of agricultural products.

The Food and Drug Administration
100
He is called the father of the Food and Drug Administration.

Harvey Washington Wiley

100

This prohibited the sale of misbranded or adulterated food and drugs in interstate commerce and laid a foundation for the nation's first consumer protection agency, FDA.

The Pure Food and Drug Act of 1906.

100

This incident involved a poisonous solvent that killed 107 people, therefore, dramatizing the need to establish drug safety

Elixir of Sulfanilamide

100

This date was when Congress passed the Pure Food and Drugs Act of 1906. 

June 30th, 1906

200

This muckraking novel instigated a public outrage at the unhygienic conditions in the Chicago stockyards, and it became a main reason why Congress established the regulatory functions of FDA.

"The Jungle"

200

This president signed the Pure Food and Drugs Act of 1906.

President Theodore Roosevelt

200

This act replaced the Pure Food and Drug Act with increased safety, required ingredient labels, and authorized inspections at factories. 

The Food, Drug, and Cosmetic Act.

200

This tragedy occurred in the late 1950’s in which the widely used drug treatment of nausea in pregnant women resulted in severe birth defects in thousands of children.

Thalidomide tragedy

200

On this year, the FDA establishes its first investigational new drug (IND) application process, laying the foundation for modern clinical trials.

1941

300

During this era, the FDA initiated a movement to replace the issues stated in the 1906 act. 

New Deal Era

300

His novel exposed the unsanitary condition of the meatpacking industry which created public outrage. This prompted Congress to improve U.S. public health and welfare.

Upton Sinclair

300

These amendments strengthened the rules for drug safety and required manufactures to prove their drugs' effectiveness. 

Kefauver-Harris Amendments

300

A program established by the FDA to ensure the protection of human subjects and the integrity of data in clinical trials.

Bioresearch Monitoring Program

300

The Food and Drug Administration Act was created this year which established the FDA as an agency of Department of Health and Human services. 

1988

400

FDA headquarters utilize this platform to inform field offices about relevant publications, speeches, changes in the agency, etc. It is a means of communicating information to state food and drug officials in order to enforce the 1906 federal act. 

The Food and Drug Review

400

This muckraking journalist studied the condition of the meat-packing industry and reported the hazards of the marketplace in vivid details. 

Samuel Hopkins

400

This act allows FDA to authorize food safety standards, which gives FDA tools to hold imported foods to the same standards as domestic foods. This act also directs FDA to partner with state and local authorities to build an integrated national food safety system. 

Food Safety and Modernization Act (FSMA)

400

This council contracted with the FDA to evaluate the effectiveness of over 4,000 drugs approved on the basis of safety between 1938-1962. 

National Academy of Sciences/National Research Council
400

On this year, the FDA launched its MedWatch program, allowing healthcare professionals and the public to report adverse events and safety concerns related to medications.

1999

500

This program was established by Congress as a successor to the Division of Chemistry in 1901. It added regulatory functions to the agency's scientific mission. 

Bureau of Chemistry
500

These groups supported the father of Food and Drug Administration. 

State chemists, food and drug inspectors, Federal Federation of Women's Club, and National Associations of Physicians and Pharmacists

500

The federal law passed by the FDA consolidated all legislation relating to the Public Health Service. It also made NCI an operating division of the National Institutes of Health. 

The Public Health Service Act of 1944
500
This board consisted of FDA staff and representatives from NIH and Veterans Administration. This board advises the Director, Center for Drug Evaluation and Research, FDA, on drug safety concerns. This board will also partner with agency in communicating safety information to health professionals and patients. 

Drug Safety Board

500

On this year, the 21st Century Cures Act was passed, aiming to accelerate the development of medical treatments and promote the use of real-world evidence in drug approvals.

2015