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Home / FDA - Page 40

FDA

FDA hired temporary investigators to prevent polio vaccine black market
FDA | Infectious Disease | Life Science History | Polio | Vaccine

FDA hired temporary investigators to prevent polio vaccine black market

On Aug. 17, 1955, the U.S. Food and Drug Administration (FDA) announced the hiring of 48 temporary investigators…

Read More FDA hired temporary investigators to prevent polio vaccine black marketContinue

The first Citizens Advisory Committee held a meeting in Washington, DC
FDA | Life Science History

The first Citizens Advisory Committee held a meeting in Washington, DC

On Feb. 3, 1955, the first Citizens Advisory Committee met in Washington, D.C. to assess the effectiveness of…

Read More The first Citizens Advisory Committee held a meeting in Washington, DCContinue

HEW Secretary Oveta Culp Hobby appointed a committee of 14 citizens to study the adequacy of FDA’s facilities and programs
FDA | Life Science History | NIH | Polio | U.S. Congress

HEW Secretary Oveta Culp Hobby appointed a committee of 14 citizens to study the adequacy of FDA’s facilities and programs

In 1955, Oveta Culp Hobby, the first Secretary of Health, Education, and Welfare (HEW) appointed a committee of…

Read More HEW Secretary Oveta Culp Hobby appointed a committee of 14 citizens to study the adequacy of FDA’s facilities and programsContinue

Hydroxychloroquine was approved for medical use in the United States
FDA | Life Science History | Therapeutics

Hydroxychloroquine was approved for medical use in the United States

In 1955, Hydroxychloroquine (HCQ) was approved for medical use in the U.S. Chloroquine was discovered in 1934 by…

Read More Hydroxychloroquine was approved for medical use in the United StatesContinue

George P Larrick becomes Commissioner of Food and Drugs
Chemistry | FDA | Life Science History

George P Larrick becomes Commissioner of Food and Drugs

On Aug. 12, 1954, George P. Larrick becomes Commissioner of Food and Drugs. In 1937, he was responsible…

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First large-scale radiological examination of food carried out by FDA
Environmental | FDA | Life Science History | Marine Science | NIH | Radiology

First large-scale radiological examination of food carried out by FDA

In 1954, first large-scale radiological examination of food carried out by U.S. Food and Drug Administration (FDA) when…

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The FDA approved methotrexate, an antimetabolite derived from folic acid, and 6-mercaptopurine as anticancer drugs
Disease | FDA | Life Science History | Therapeutics

The FDA approved methotrexate, an antimetabolite derived from folic acid, and 6-mercaptopurine as anticancer drugs

On Dec. 7, 1953, the U.S. Food and Drug Administration (FDA) approved Dava Pharmaceuticals’ methotrexate oral tablet, an…

Read More The FDA approved methotrexate, an antimetabolite derived from folic acid, and 6-mercaptopurine as anticancer drugsContinue

Factory Inspection Amendment required FDA to give manufacturers written reports of conditions observed during inspections
FDA | Life Science History | U.S. Congress

Factory Inspection Amendment required FDA to give manufacturers written reports of conditions observed during inspections

In 1953, the U.S. Congress enacted the Factory Inspection Amendment which clarified previous law and required the U.S….

Read More Factory Inspection Amendment required FDA to give manufacturers written reports of conditions observed during inspectionsContinue

The Supreme Court ruled the factory inspection provision of the 1938 FDC Act was too vague to be enforced
FDA | Life Science History

The Supreme Court ruled the factory inspection provision of the 1938 FDC Act was too vague to be enforced

On Dec. 8, 1952, in U.S. v. Cardiff, the Supreme Court ruled that the factory inspection provision of…

Read More The Supreme Court ruled the factory inspection provision of the 1938 FDC Act was too vague to be enforcedContinue

FDA consumer consultants appointed in each field district to maintain communications with consumers
FDA | Life Science History

FDA consumer consultants appointed in each field district to maintain communications with consumers

In November, 1952, U.S. Food and Drug Administration (FDA) consumer consultants were appointed in each field district to…

Read More FDA consumer consultants appointed in each field district to maintain communications with consumersContinue

Dr. William Hammon conducted the first placebo-controlled field trial of gamma globulin in Provo, Utah
FDA | Life Science History | Polio | Vaccine

Dr. William Hammon conducted the first placebo-controlled field trial of gamma globulin in Provo, Utah

In September 1952, Dr. William Hammon conducted the first placebo-controlled field trial of gamma globulin that, in just…

Read More Dr. William Hammon conducted the first placebo-controlled field trial of gamma globulin in Provo, UtahContinue

Alfred Hershey and Martha Chase verified genes were made of DNA
Disease | FDA | Life Science History | Medicine | Oncology | Pharmaceutical | Radiology

Alfred Hershey and Martha Chase verified genes were made of DNA

In 1952, Alfred Hershey and Martha Chase conducted a series of experiments at the Carnegie Institute of Washington…

Read More Alfred Hershey and Martha Chase verified genes were made of DNAContinue

The U.S. Food and Drug Administration approved the use of antibiotics on animals
FDA | Life Science History | Veterinary

The U.S. Food and Drug Administration approved the use of antibiotics on animals

In 1951, the U.S. Food and Drug Administration (FDA) approved the use of antibiotics on animals. In 1943, farmers…

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The FDA approved nitrogen mustard (mechlorethamine) to kill cancer cells
FDA | Life Science History | Oncology

The FDA approved nitrogen mustard (mechlorethamine) to kill cancer cells

In 1949, the U.S. Food and Drug Administration (FDA) approved nitrogen mustard to kill cancer cells. The major use…

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FDA published guidance to industry known as the “black book”
Biotechnology | Chemistry | FDA | Life Science History | Therapeutics

FDA published guidance to industry known as the “black book”

In 1949, U.S. Food and Drug Administration (FDA) published guidance to industry for the first time. This guidance,…

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Combination diphtheria and tetanus toxoids for pediatric use was first licensed in the U.S.
CDC | FDA | Life Science History | Vaccine

Combination diphtheria and tetanus toxoids for pediatric use was first licensed in the U.S.

In 1947, a combination diphtheria and tetanus toxoids for pediatric use was first licensed in the U.S. After…

Read More Combination diphtheria and tetanus toxoids for pediatric use was first licensed in the U.S.Continue

The Oklahoma Medical Research Foundation articles of incorporation were signed
Biology | Diagnostics | Disease | FDA | Life Science History | Non-Profit Research | Therapeutics

The Oklahoma Medical Research Foundation articles of incorporation were signed

On Aug. 3, 1946, the articles of incorporation were signed by Governor Roy J. Turner that established the…

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fluoride First Used in U.S. Public water Supply
Chemistry | Dentistry | Diagnostics | Disease | Environmental | FDA | Life Science History | Therapeutics

fluoride First Used in U.S. Public water Supply

On Jan. 25, 1945, at 4:00 p.m., Grand Rapids, Michigan, achieved a historic milestone by becoming the inaugural…

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Penicillin Amendment required FDA testing and certification of safety and effectiveness of all penicillin products
Biology | FDA | Life Science History | Therapeutics | U.S. Congress

Penicillin Amendment required FDA testing and certification of safety and effectiveness of all penicillin products

In 1945, the U.S. Congress passed the Penicillin Amendment, modeled on the earlier Insulin Amendment. The former required…

Read More Penicillin Amendment required FDA testing and certification of safety and effectiveness of all penicillin productsContinue

Paul B. Dunbar, PhD, became Commissioner of Food and Drugs
Disease | FDA | Life Science History | Medicine | Vaccine

Paul B. Dunbar, PhD, became Commissioner of Food and Drugs

On May. 1, 1944, Paul B. Dunbar, Ph.D., becomes Commissioner of Food and Drugs. His tenure as commissioner…

Read More Paul B. Dunbar, PhD, became Commissioner of Food and DrugsContinue

Chemotherapy was first used to treat a cancer patient
Chemistry | FDA | Life Science History | Oncology | Therapeutics

Chemotherapy was first used to treat a cancer patient

On Aug. 27, 1942, chemotherapy was first used to treat a cancer patient and the beginning of its…

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Insulin Advisory Committee announced the development of a USP Reference Standard for insulin
FDA | Life Science History

Insulin Advisory Committee announced the development of a USP Reference Standard for insulin

On Dec. 1, 1941, in response to the emergency need for insulin standards, the USP formed an Insulin…

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U.S. Congress passed the Federal Food, Drug, and Cosmetic Act
Biology | FDA | Life Science History | Medicine | NIH | Pharmaceutical | Therapeutics | U.S. Congress

U.S. Congress passed the Federal Food, Drug, and Cosmetic Act

On Jun. 25, 1938, the U.S. Congress passed the Federal Food, Drug, and Cosmetic Act with new provisions….

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The Federal Trade Commission was charged with overseeing advertising associated with products otherwise regulated by FDA
FDA | Life Science History | U.S. Congress

The Federal Trade Commission was charged with overseeing advertising associated with products otherwise regulated by FDA

In 1938, under the Wheeler-Lea Act passed by the U.S. Congress, the Federal Trade Commission is charged with…

Read More The Federal Trade Commission was charged with overseeing advertising associated with products otherwise regulated by FDAContinue

Influenza vaccine developed to protect U.S. military forces
FDA | Infectious Disease | Influenza | Life Science History | U.S. Congress | Vaccine

Influenza vaccine developed to protect U.S. military forces

In 1938, Thomas Francis, Jr., MD and Jonas Salk, MD served as lead researchers at the University of…

Read More Influenza vaccine developed to protect U.S. military forcesContinue

U.S. Congress investigated the Elixir Sulfanilamide tragedy that poisoned more than 100 people
Diagnostics | FDA | Life Science History | Medicine | U.S. Congress

U.S. Congress investigated the Elixir Sulfanilamide tragedy that poisoned more than 100 people

On Nov. 16, 1937, the U.S. Congress directed the Food and Drug Administration (FDA) to give a full…

Read More U.S. Congress investigated the Elixir Sulfanilamide tragedy that poisoned more than 100 peopleContinue

A bill was introduced in the U.S. Senate to overhaul the 1906 drug law
FDA | Life Science History | Medicine | U.S. Congress

A bill was introduced in the U.S. Senate to overhaul the 1906 drug law

On Jun. 12, 1933, a bill was introduced in the U.S. Senate by New York Senator Royal S….

Read More A bill was introduced in the U.S. Senate to overhaul the 1906 drug lawContinue

The FDA recommended a complete revision of the obsolete 1906 Food and Drugs Act
FDA | Life Science History | Medicine | U.S. Congress

The FDA recommended a complete revision of the obsolete 1906 Food and Drugs Act

In 1933, the U.S. Food and Drug Administration (FDA) recommended a complete revision of the obsolete 1906 Food and…

Read More The FDA recommended a complete revision of the obsolete 1906 Food and Drugs ActContinue

McNary-Mapes Amendment to the Pure Food and Drugs Act was passed
FDA | Life Science History

McNary-Mapes Amendment to the Pure Food and Drugs Act was passed

On May 7, 1930, the McNary-Mapes Amendment to the Pure Food and Drugs Act was passed. The so-called…

Read More McNary-Mapes Amendment to the Pure Food and Drugs Act was passedContinue

The name of the Food, Drug, and Insecticide Administration was shortened to Food and Drug Administration
Agriculture | Diagnostics | Disease | FDA | Life Science History | Therapeutics | U.S. Congress

The name of the Food, Drug, and Insecticide Administration was shortened to Food and Drug Administration

In 1930, the name of the Food, Drug, and Insecticide Administration was shortened to Food and Drug Administration…

Read More The name of the Food, Drug, and Insecticide Administration was shortened to Food and Drug AdministrationContinue

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