Zdrowie i gospodarka · 04/12/2014

FDA Updates Labeling Requirements for Human Prescription Drugs and Biological Products During Pregnancy and Lactation

The US Food and Drug Administration (FDA) has amended its regulations to simplify labeling for human prescription drugs and biological products, removing outdated pregnancy categories and requiring more detailed information on risks and prescribing decisions during pregnancy and lactation.

Source: Federal Register — Food and Drug AdministrationOpen original release →

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