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 Vol 6: Analytical Challenges and Regulatory Requirements for Nasal Drug Products in Europe and the U.S.


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This article is from Pharmaceutics, volume 6.AbstractNasal drug delivery can be assessed by a variety of means and regulatory agencies, e.g., the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have published a set of guidelines and regulations proposing in vitro test methods for the characterization of nasal drug product

Autor: Trows, Sabrina; Wuchner, Klaus; Spycher, Rene; Steckel, Hartwig

Fuente: https://archive.org/







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