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Zdrowie i gospodarka · 14/03/2014

FDA Releases Draft Guidance on Injectable Drug and Biological Products Packaging

The Food and Drug Administration (FDA) has published a draft guidance document outlining the agency's requirements for allowable excess volume and labeled vial fill size in injectable drug and biological products, aiming to clarify and standardize packaging sizes for these products.

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