Zdrowie i gospodarka · 24/01/2006

FDA Releases Draft Guidances for Human Prescription Drug Labeling

The Food and Drug Administration (FDA) has released two draft guidances to help pharmaceutical companies comply with new labeling requirements for human prescription drugs and biological products. The guidelines cover the content and format of labeling, warnings, and boxed warnings sections.

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

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