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Regulatory Requirements for the Development of Second-Entry Semisolid Topical Products in the European Union.
García-Arieta, Alfredo; Gordon, John; Gwaza, Luther; Merino, Virginia; Mangas-Sanjuan, Víctor.
Afiliação
  • García-Arieta A; Área de Farmacocinética y Medicamentos Genéricos, División de Farmacología y Evaluación Clínica, Departamento de Medicamentos de Uso Humano, Agencia Española de Medicamentos y Productos Sanitarios, 28022 Madrid, Spain.
  • Gordon J; Division of Biopharmaceutics Evaluation, Bureau of Pharmaceutical Sciences, Pharmaceutical Drugs Directorate, Health Canada, Ottawa, ON K1A 0K9, Canada.
  • Gwaza L; Norms and Standards for Pharmaceuticals, Health Products Policy and Standards, Access to Medicines and Health Products Division, World Health Organization, 1211 Geneva, Switzerland.
  • Merino V; Department of Pharmacy and Pharmaceutical Technology and Parasitology, University of Valencia, 46100 Valencia, Spain.
  • Mangas-Sanjuan V; Interuniversity Research Institute for Molecular Recognition and Technological Development, Polytechnic University of Valencia-University of Valencia, 46022 Valencia, Spain.
Pharmaceutics ; 15(2)2023 Feb 10.
Article em En | MEDLINE | ID: mdl-36839924
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Espanha
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Espanha