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Zdrowie i gospodarka · 05/01/1999

FDA Releases Draft Guidance for Industry on SUPAC-SS Addendum for Nonsterile Semisolid Dosage Forms

The FDA has made available a draft guidance document for pharmaceutical manufacturers, outlining recommendations for manufacturing nonsterile semisolid dosage forms, building on the existing SUPAC-SS guidance.

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