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Home / FDA - Page 38

FDA

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 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

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

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
FDA | Life Science History

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 recommended systematic review of GRAS…

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

FDA formed the Drug Efficacy Study Implementation
Disease | FDA | Life Science History | Medicine | Pharmaceutical | U.S. Congress

FDA formed the Drug Efficacy Study Implementation

In 1968, the U.S. Food and Drug Administration (FDA) formed the Drug Efficacy Study Implementation (DESI) to implement recommendations…

Read More FDA formed the Drug Efficacy Study ImplementationContinue

Medtronic annual sales skyrocketed to more than $12 million
FDA | Life Science History | Medical Device | Therapeutics

Medtronic annual sales skyrocketed to more than $12 million

In 1968, Medtronic annual sales skyrocketed to more than $12 million, with the company reporting net income in…

Read More Medtronic annual sales skyrocketed to more than $12 millionContinue

Mumps virus vaccine live (MumpsVax by Merck) was licensed
FDA | Infectious Disease | Life Science History | Vaccine

Mumps virus vaccine live (MumpsVax by Merck) was licensed

On Dec. 28, 1967, the U.S. Food and Drug Administration (FDA) approved Mercks mumps virus vaccine live (MumpsVax)….

Read More Mumps virus vaccine live (MumpsVax by Merck) was licensedContinue

Fair Packaging and Labeling Act required all consumer products in interstate commerce to be honestly and informatively labeled
FDA | Life Science History | Medical Device | Medicine | Pharmaceutical | U.S. Congress

Fair Packaging and Labeling Act required all consumer products in interstate commerce to be honestly and informatively labeled

In 1967 the Fair Packaging and Labeling Act (FPLA or Act), enacted by the U.S. Congress directs the…

Read More Fair Packaging and Labeling Act required all consumer products in interstate commerce to be honestly and informatively labeledContinue

Medtronic introduced two “on-demand” pacemakers
FDA | Life Science History | Medical Device

Medtronic introduced two “on-demand” pacemakers

In 1967, Medtronic introduced two “on-demand” pacemakers, designed to avoid competition between paced beats and the patient’s own…

Read More Medtronic introduced two “on-demand” pacemakersContinue

The Child Protection Act was passed by the U.S. Congress
Chemistry | FDA | Life Science History | U.S. Congress

The Child Protection Act was passed by the U.S. Congress

On Nov. 3, 1966, the Child Protection Act was passed by the U.S. Congress. The bill enlarged the…

Read More The Child Protection Act was passed by the U.S. CongressContinue

FDA contracted with National Academy of Sciences to evaluate effectiveness of drugs
FDA | Life Science History | Medicine | NIH | Therapeutics | U.S. Congress

FDA contracted with National Academy of Sciences to evaluate effectiveness of drugs

In 1966, the Drug Efficacy Study of the National Research Council’s Division of Medical Sciences, which was tasked…

Read More FDA contracted with National Academy of Sciences to evaluate effectiveness of drugsContinue

Diagnostics | FDA | Infectious Disease | Influenza | Life Science History | Medicine

The FDA licensed amantadine, a new antiviral medication, as a prophylactic against influenza A

In 1966, the U.S. Food and Drug Administration (FDA) licensed amantadine (marketed as Symmetrel) to Du Pont, a…

Read More The FDA licensed amantadine, a new antiviral medication, as a prophylactic against influenza AContinue

FDA requested help in removing “X-33 Water Repellent” from the market
Disease | Environmental | FDA | Life Science History

FDA requested help in removing “X-33 Water Repellent” from the market

On Aug. 30, 1964, the U.S. Food and Drug Administration (FDA) requested help in removing “X-33 Water Repellent”…

Read More FDA requested help in removing “X-33 Water Repellent” from the marketContinue

The anticancer drug melphalan (L-PAM) was approved by the FDA
Biology | FDA | Life Science History | Medicine | Oncology | Therapeutics

The anticancer drug melphalan (L-PAM) was approved by the FDA

In 1964, the anticancer drug melphalan (L-PAM) was approved by the U.S. Food and Drug Administration.

Read More The anticancer drug melphalan (L-PAM) was approved by the FDAContinue

The anticancer drug Azidothymidine (AZT) was synthesized in Michigan Cancer Foundation’s chemistry lab
Chemistry | FDA | HIV | Life Science History | Oncology

The anticancer drug Azidothymidine (AZT) was synthesized in Michigan Cancer Foundation’s chemistry lab

In 1964, the anticancer drug Azidothymidine (AZT) was synthesized in Michigan Cancer Foundation’s chemistry lab by Jerome Horwitz,…

Read More The anticancer drug Azidothymidine (AZT) was synthesized in Michigan Cancer Foundation’s chemistry labContinue

The U.S. FDA approved vincristine, a sister drug to vinblastine
FDA | Life Science History | U.S. Congress

The U.S. FDA approved vincristine, a sister drug to vinblastine

On Jul. 10, 1963, the U.S. FDA approved vincristine, a sister drug to vinblastine. The drug was established…

Read More The U.S. FDA approved vincristine, a sister drug to vinblastineContinue

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