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The scope of pharmacy practice includes more traditional roles such as compounding and dispensing medications, and it also includes more modern services
In the U.S., the government’s Food and Drug Administration (FDA) must approve any drug – whether it’s prescription or over-the-counter – before it can be sold. The FDA evaluates the safety of a drug by looking at side effects, how it’s manufactured, results of animal testing and clinical trials, and more. The FDA also monitors a drug’s safety after approval.
When a pharmaceutical company first develops a medicine, it takes out a patent to make sure it has the exclusive right to produce and market the medicine with a particular active ingredient. The active ingredient is the chemical in the medicine that makes the medicine work. These original medicines are often marketed under the pharmaceutical company�s trade-marked name and can be called the �originator brand� or the �branded� medicine.
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