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

• Principais autores: Sabrina Trows (Autor), Klaus Wuchner (Autor), Rene Spycher (Autor), Hartwig Steckel (Autor)
• Formato: Livro
• Publicado em: MDPI AG, 2014-04-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

Nasal 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 products....