How has the regulation of pharmaceuticals changed over time?

The regulation of pharmaceuticals has changed over time, and this is especially true in the state of New York. In the 19th century, New York began requiring all prescriptions to be written by a licensed doctor or pharmacist and for those prescriptions to be filled from a licensed druggist. Pharmaceuticals were only allowed to be sold after they were tested and approved by the state. In the early 20th century, New York passed a law that required all new or investigational drugs receive approval from the State Board of Pharmacy before they could be sold. This law also required that drug manufacturers submit evidence verifying the safety of the drug prior to approval. In recent years, as technology has become more advanced, the regulation and control of pharmaceuticals has become even stricter in New York. The state has implemented stricter labeling requirements, packaging requirements, and prescribing guidelines for pharmaceuticals. Further, manufacturers are now required to provide more detailed information about the drug, such as its side effects, interactions, and other risks. Overall, it is clear that the regulation of pharmaceuticals in New York has come a long way. As medical technology advances, these regulations have become tighter and more specific, ensuring that the drugs being sold in New York are safe and effective for consumers.

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How has the regulation of pharmaceuticals changed over time?

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