Add to ORKGFood and Drug Administration (FDA) rules are often forged in crisis. After the 1937 sulfanilamide disaster that killed more than 100 people, Congress passed the Food, Drug, and Cosmetic Act (FDCA),requiring drugs to be safe and properly labeled. In 1962, a requirement was introduced for proof of drug efficacy through “adequate and well-controlled investigations,” partly in response to the thalidomide tragedy. Rules protecting human-research subjects owe a debt to Tuskegee and Nuremberg
For most of its existence, the Food and Drug Administration (FDA) has acted as the ultimate arbiter ...
Last year alone, doctors filled out over four billion drug prescriptions in the United States. But a...
In 1938 the Food and Drug Administration (FDA) adopted regulations which created a category of presc...
Food and Drug Administration (FDA) rules are often forged in crisis. After the 1937 sulfanilamide di...
After the compounding pharmacy disaster at New England Compounding Center, Congress had an opportuni...
On November 27, 2013, President Obama signed into law the Drug Quality and Security Act ( DQSA ), wh...
For many years, the art of pharmaceutical compounding in the United States has been largely an overl...
On May 22. 2013, the Senate Health, Education, Labor and Pensions (HELP) Committee unanimously appro...
In late 2012 and early 2013, tainted steroid shots from the New England Compounding Center ( NECC ) ...
Pharmaceutical compounding, the creation and dispensing of custom-made medications, is the root of t...
Federal regulation of the traditional art of pharmacy practice compounding is an unsettled area of t...
For much of the last half-century, the Food and Drug Administration has earned a reputation as one o...
Compounding is the act of combining, mixing or altering ingredients to create a drug tailored to the...
A letter report issued by the Government Accountability Office with an abstract that begins "The aut...
Pharmaceutical compounding is the com-bining, mixing, or altering of ingredients to create a customi...
For most of its existence, the Food and Drug Administration (FDA) has acted as the ultimate arbiter ...
Last year alone, doctors filled out over four billion drug prescriptions in the United States. But a...
In 1938 the Food and Drug Administration (FDA) adopted regulations which created a category of presc...
Food and Drug Administration (FDA) rules are often forged in crisis. After the 1937 sulfanilamide di...
After the compounding pharmacy disaster at New England Compounding Center, Congress had an opportuni...
On November 27, 2013, President Obama signed into law the Drug Quality and Security Act ( DQSA ), wh...
For many years, the art of pharmaceutical compounding in the United States has been largely an overl...
On May 22. 2013, the Senate Health, Education, Labor and Pensions (HELP) Committee unanimously appro...
In late 2012 and early 2013, tainted steroid shots from the New England Compounding Center ( NECC ) ...
Pharmaceutical compounding, the creation and dispensing of custom-made medications, is the root of t...
Federal regulation of the traditional art of pharmacy practice compounding is an unsettled area of t...
For much of the last half-century, the Food and Drug Administration has earned a reputation as one o...
Compounding is the act of combining, mixing or altering ingredients to create a drug tailored to the...
A letter report issued by the Government Accountability Office with an abstract that begins "The aut...
Pharmaceutical compounding is the com-bining, mixing, or altering of ingredients to create a customi...
For most of its existence, the Food and Drug Administration (FDA) has acted as the ultimate arbiter ...
Last year alone, doctors filled out over four billion drug prescriptions in the United States. But a...
In 1938 the Food and Drug Administration (FDA) adopted regulations which created a category of presc...