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FDA Revisits Botanical Drugs

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In Short: The FDA is reassessing its approach to botanical drugs as part of its ongoing efforts to improve drug regulation.

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Photo: Drug Enforcement Administration / Wikimedia Commons (Public domain)

The U.S. Food and Drug Administration (FDA) is currently reviewing its policies on botanical drugs, a move aimed at enhancing the regulatory framework for these medications.

This reassessment comes as part of the FDA's broader strategy to address persistent challenges in the pharmaceutical industry, including the barriers to the use of clozapine and the potential of pig kidneys in bridging the gap for organ transplant patients.

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