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Research / Pharmaceutical sciences / Health / Committee for Medicinal Products for Human Use / Directive 2001/83/EC / Summary of Product Characteristics / Medicinal product / European Medicines Agency / Pharmacology / Pharmaceuticals policy / Clinical research


Human Medicines - EMEA Pre-Submission Procedural Advice How will I know if the proposed invented name of my medicinal product is acceptable from a public health point of view? In accordance with Article 6 of Regulation (
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Document Date: 2008-06-27 10:21:48

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Name Review Group / /

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IndustryTerm

pharmaceutical connotations / medicinal product / biological medicinal products / authorisation applications / human medicinal products / authorisations/applications / non-prescription medicinal products / medicinal products / marketing authorisation applications / /

Organization

World Health Organisation / NRG Secretariat / European Union / EMEA Secretariat / European Commission / /

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Volume / /

Position

EMEA representative / /

ProgrammingLanguage

EC / /

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