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Home / FDA - Page 38

FDA

Tamoxifen was approved by the FDA for the treatment of breast cancer
Biotechnology | Diagnostics | Disease | FDA | Oncology | Radiology | Therapeutics | Women's Health

Tamoxifen was approved by the FDA for the treatment of breast cancer

On Dec. 30, 1977, the U.S. Food and Drug Administration approved Tamoxifen, an anti-estrogen drug, for the treatment…

Read More Tamoxifen was approved by the FDA for the treatment of breast cancerContinue

Saccharin Study and Labeling Act passed by Congress to stop FDA from banning the chemical sweetener
Chemistry | FDA | Life Science History | U.S. Congress

Saccharin Study and Labeling Act passed by Congress to stop FDA from banning the chemical sweetener

On Nov. 23, 1977, the Saccharin Study and Labeling Act was enacted by the U.S. Congress to stop…

Read More Saccharin Study and Labeling Act passed by Congress to stop FDA from banning the chemical sweetenerContinue

The first pneumococcal vaccine was licensed
FDA | Infectious Disease | Vaccine

The first pneumococcal vaccine was licensed

On Nov. 21, 1977, the U.S. Food and Drug Administration (FDA) licensed the first pneumococcal vaccine containing 14…

Read More The first pneumococcal vaccine was licensedContinue

Donald Kennedy, Ph.D., became Commissioner of Food and Drugs
FDA | Life Science History

Donald Kennedy, Ph.D., became Commissioner of Food and Drugs

On Apr. 4, 1977, Donald Kennedy, Ph.D., became Commissioner of the U.S. Food and Drug Administration (FDA). Kennedy,…

Read More Donald Kennedy, Ph.D., became Commissioner of Food and DrugsContinue

The U.S. FDA Bioresearch Monitoring Program was introduced
Biotechnology | FDA | Life Science History | Therapeutics

The U.S. FDA Bioresearch Monitoring Program was introduced

In 1977, the U.S. Food and Drug Administration (FDA) established the Bioresearch Monitoring Program (BiMo) to develop cross-center…

Read More The U.S. FDA Bioresearch Monitoring Program was introducedContinue

Vitamin-Mineral Amendment to the Federal Food, Drug, and Cosmetic Act was passed
FDA | Life Science History | U.S. Congress

Vitamin-Mineral Amendment to the Federal Food, Drug, and Cosmetic Act was passed

On Apr. 22, 1976, the U.S. Congress passed the Vitamin-Mineral Amendment to the Federal Food, Drug, and Cosmetic…

Read More Vitamin-Mineral Amendment to the Federal Food, Drug, and Cosmetic Act was passedContinue

H1N1 outbreak at Fort Dix lead to a vaccination program to prevent a pandemic
Biotechnology | CDC | Diagnostics | FDA | Influenza | Life Science History | Therapeutics | Vaccine

H1N1 outbreak at Fort Dix lead to a vaccination program to prevent a pandemic

In 1976, Influenza A/Victoria-like strains had been identified in New Jersey as early as January 21. The novel…

Read More H1N1 outbreak at Fort Dix lead to a vaccination program to prevent a pandemicContinue

U.S. Congress passed Medical Device Amendments to ensure safety and effectiveness of medical devices
Diagnostics | FDA | Life Science History | Medical Device | Therapeutics | U.S. Congress

U.S. Congress passed Medical Device Amendments to ensure safety and effectiveness of medical devices

In 1976, the U.S. Congress passed the Medical Device Amendments to ensure safety and effectiveness of medical devices,…

Read More U.S. Congress passed Medical Device Amendments to ensure safety and effectiveness of medical devicesContinue

Rapamcyin, an immune suppression drug, was isolated from a soil sample from Easter Island
FDA | Life Science History | Medicine | Therapeutics

Rapamcyin, an immune suppression drug, was isolated from a soil sample from Easter Island

In 1975, rapamycin, a macrolide produced by the bacterium Streptomyces hygroscopicus was first discovered and isolated from soil…

Read More Rapamcyin, an immune suppression drug, was isolated from a soil sample from Easter IslandContinue

University of Iowa began pharmaceutical production
Biotechnology | CMO | FDA | Life Science History | Non-Profit Research | Pharmaceutical

University of Iowa began pharmaceutical production

In Jul. 1974, In the Division of Pharmaceutical Service at the University of Iowa began producing cGMP compliant…

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The FDA approved doxorubicin (Adriamycin)
FDA | Life Science History | Oncology | Therapeutics

The FDA approved doxorubicin (Adriamycin)

In 1974, the U.S. Food and Drug Administration (FDA) approved doxorubicin (Adriamycin), an antitumor anthracycline antibiotic from Streptomyces…

Read More The FDA approved doxorubicin (Adriamycin)Continue

U.S. Supreme Court upheld 1962 drug effectiveness law and endorsed FDA action to control products by regulation
FDA | Life Science History | Medicine | Pharmaceutical | Therapeutics | U.S. Congress

U.S. Supreme Court upheld 1962 drug effectiveness law and endorsed FDA action to control products by regulation

On Jun. 18, 1973, the U.S. Supreme Court upheld the 1962 drug effectiveness law and endorsed Food and…

Read More U.S. Supreme Court upheld 1962 drug effectiveness law and endorsed FDA action to control products by regulationContinue

U.S. FDA issued low-acid food processing regulations after botulism outbreaks from canned foods
Biology | Disease | FDA

U.S. FDA issued low-acid food processing regulations after botulism outbreaks from canned foods

On Feb. 17, 1973, the  U.S. Food and Drug Administration (FDA) announced the recall of 29,500 institutional-size cans of…

Read More U.S. FDA issued low-acid food processing regulations after botulism outbreaks from canned foodsContinue

Consumer Product Safety Commission was enacted by Congress
Chemistry | FDA | Life Science History | U.S. Congress

Consumer Product Safety Commission was enacted by Congress

On Oct. 27, 1972, the Consumer Product Safety Commission (CPSA) was enacted by the U.S. Congress. The CPSA…

Read More Consumer Product Safety Commission was enacted by CongressContinue

Regulation of Biologics–including serums, vaccines, and blood products–was transferred from NIH to FDA
FDA | Life Science History | NIH

Regulation of Biologics–including serums, vaccines, and blood products–was transferred from NIH to FDA

On Jul. 1, 1972, the Regulation of Biologics–including serums, vaccines, and blood products–was transferred from the NIH to…

Read More Regulation of Biologics–including serums, vaccines, and blood products–was transferred from NIH to FDAContinue

The Division of Biologics Standards was transferred from NIH to FDA
FDA | Life Science History | NIH

The Division of Biologics Standards was transferred from NIH to FDA

In 1972, the Division of Biologics Standards was transferred from the National Institutes of Health (NIH)  to the U.S….

Read More The Division of Biologics Standards was transferred from NIH to FDAContinue

The FDA began to regulate all 7,000 US blood and plasma centers
Biology | FDA | Life Science History | Therapeutics

The FDA began to regulate all 7,000 US blood and plasma centers

In 1972, the Food and Drug Administration’s (FDA) new Bureau of Biologics began to regulate all 7000 U.S….

Read More The FDA began to regulate all 7,000 US blood and plasma centersContinue

Artificial sweetener saccharin removed from FDA’s original GRAS list pending new scientific study
FDA | Life Science History

Artificial sweetener saccharin removed from FDA’s original GRAS list pending new scientific study

On Sept. 29, 1971, the artificial sweetener saccharin, included in FDA’s original GRAS list, was removed from the…

Read More Artificial sweetener saccharin removed from FDA’s original GRAS list pending new scientific studyContinue

The Public Health Service’s Bureau of Radiological Health was transferred to the FDA
FDA | Life Science History

The Public Health Service’s Bureau of Radiological Health was transferred to the FDA

On May 17, 1971, The Public Health Service’s Bureau of Radiological Health was transferred to the FDA.

Read More The Public Health Service’s Bureau of Radiological Health was transferred to the FDAContinue

PHS Bureau of Radiological Health was transferred to FDA
FDA | NIH | Radiology | Therapeutics

PHS Bureau of Radiological Health was transferred to FDA

In 1971, the Public Health Service (PHS) Bureau of Radiological Health was transferred to U.S. Food and Drug…

Read More PHS Bureau of Radiological Health was transferred to FDAContinue

Court of Appeals ruled commercial success does not constitute substantial evidence of drug safety and efficacy
FDA | Life Science History | Pharmaceutical | U.S. Congress

Court of Appeals ruled commercial success does not constitute substantial evidence of drug safety and efficacy

On Feb. 27, 1970, in Upjohn v. Finch the Court of Appeals upheld enforcement of the 1962 drug…

Read More Court of Appeals ruled commercial success does not constitute substantial evidence of drug safety and efficacyContinue

FDA required the first patient package insert: oral contraceptives must contain information for the patient about specific risks and benefits
Biology | FDA | Women's Health

FDA required the first patient package insert: oral contraceptives must contain information for the patient about specific risks and benefits

In 1970, the U.S. Food and Drug Administration (FDA) required the first patient package insert: oral contraceptives must contain…

Read More FDA required the first patient package insert: oral contraceptives must contain information for the patient about specific risks and benefitsContinue

Charles Edwards, MD, became FDA commissioner
FDA | Life Science History

Charles Edwards, MD, became FDA commissioner

On Dec. 13, 1969, Charles Edwards, M.D., becomes FDA commissioner.

Read More Charles Edwards, MD, became FDA commissionerContinue

The White House Conference on Food, Nutrition, and Health recommended systematic review of GRAS substances
Agriculture | Biotechnology | FDA | Life Science History | Non-Profit Research | U.S. Congress

The White House Conference on Food, Nutrition, and Health recommended systematic review of GRAS substances

On Dec. 2, 1969, the White House Conference on Food, Nutrition, and Health (WHC) was a seminal event…

Read More The White House Conference on Food, Nutrition, and Health recommended systematic review of GRAS substancesContinue

FDA issued report that declared birth control pills “safe”
FDA | Life Science History

FDA issued report that declared birth control pills “safe”

On Sept. 4, 1969, the FDA issued a report that called birth control pills safe, despite a slight…

Read More FDA issued report that declared birth control pills “safe”Continue

FDA began administering Sanitation Programs for milk, shellfish, food service, and interstate travel facilities
Agriculture | Biology | Diagnostics | Disease | FDA

FDA began administering Sanitation Programs for milk, shellfish, food service, and interstate travel facilities

In 1969, the U.S. Food and Drug Administration (FDA) began administering Sanitation Programs for milk, shellfish, food service, and…

Read More FDA began administering Sanitation Programs for milk, shellfish, food service, and interstate travel facilitiesContinue

The CDC began a national rubella immunization campaign
CDC | FDA | Infectious Disease | Life Science History | Measles | Vaccine

The CDC began a national rubella immunization campaign

In 1969, live, attenuated rubella vaccines were first licensed in the U.S., and a vaccination program was established…

Read More The CDC began a national rubella immunization campaignContinue

A second live, further attenuated measles virus vaccine was licensed
FDA | Infectious Disease | Life Science History | Measles | Vaccine

A second live, further attenuated measles virus vaccine was licensed

On Nov. 26, 1968, the U.S. Food and Drug Administration (FDA) licensed a second live, further attenuated measles…

Read More A second live, further attenuated measles virus vaccine was licensedContinue

FDA | Life Science History

FDA Bureau of Drug Abuse Control and Treasury Department Bureau of Narcotics were transferred to Dept of Justice

On Apr. 7, 1968, the FDA Bureau of Drug Abuse Control and Treasury Department Bureau of Narcotics were…

Read More FDA Bureau of Drug Abuse Control and Treasury Department Bureau of Narcotics were transferred to Dept of JusticeContinue

Reorganization of federal health programs placed FDA in the Public Health Service
Environmental | FDA | Life Science History

Reorganization of federal health programs placed FDA in the Public Health Service

In March 1968, a reorganization of federal health programs placed the U.S. Food and Drug Administration (FDA) in…

Read More Reorganization of federal health programs placed FDA in the Public Health ServiceContinue

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