The future of American drug innovation is threatened by U.S. regulations that permit knockoff versions of new drugs to be ...
THE Anti-Red Tape Authority (ARTA) said that it will recommend to the Food and Drug Administration (FDA) to make pre-assessment a part of the 3-7-20 standard processing time. “We just had our workshop ...
The United States has led the world in pharmaceutical innovation for decades by developing drugs that combat cancer, heart ...
Fosamax further defines the obligation of drug manufacturers to present clear, unambiguous, and accurate information to the ...
The Food and Drugs Authority (FDA) has intercepted 120 boxes of unregistered Hepatitis B vaccines at Aflao on the Ghana-Togo ...
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GlobalData on MSNUFlex receives FDA approval for recycled polyethylene in food packagingThe move marks an advancement in reducing plastic waste and assisting global brands in achieving their sustainability ...
The future of American drug innovation is threatened by US regulations that permit knockoff versions of new drugs to be sold ...
He founded the Preventing Tobacco Addiction Foundation in 1996 and began to push for state legislatures to raise the tobacco sales age. At first, he had scant success. But in 2003, a town in ...
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The Food and Drug Administration permits companies to use lead, arsenic, and other dangerous heavy metals (PDF) in things ...
A former commissioner of the Food and Drug Administration says it is vital to invest in ensuring infant formula and breast milk banks are inspected rigorously.
When there is a shortage of a branded medication, the FDA permits compounding pharmacies to produce copycat versions. In most situations, the manufacturing of these treatments is done piecemeal.
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