European Medicines Agency

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• European Medicines Agency — European Medicines Agency …   Wikipedia

• European medicines agency — Die Europäische Arzneimittelagentur (engl. European Medicines Agency, abk. EMEA) ist eine Agentur der Europäischen Union mit Sitz in London, die für die Beurteilung und Überwachung von Arzneimitteln zuständig ist. Der EMEA obliegt die Erhaltung… …   Deutsch Wikipedia

• European medicines agency — Agence européenne des médicaments Agence européenne des médicaments …   Wikipédia en Français

• European Environment Agency — European Environment Agency …   Wikipedia

• Agency of the European Union — European Union This article is part of the series: Politics and government of the European Union …   Wikipedia

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• European Ombudsman — European Union The European Ombudsman investigates complaints about maladministration in the institutions and bodies of the European Union. The institutions include, among others, the European Commission, the Council of the EU and the European… …   Law dictionary

• Medicines and Healthcare products Regulatory Agency — The logo of the MHRA. The Medicines and Healthcare products Regulatory Agency (MHRA) is the UK government agency which is responsible for ensuring that medicines and medical devices work and are acceptably safe. The agency was formed on 1 April… …   Wikipedia

• European Directorate for the Quality of Medicines — The European Directorate for the Quality of Medicines of the Council of Europe (EDQM) came into being in its current form in 1996. It consists of the Technical Secretariat of the European Pharmacopoeia Commission long referred to as the European… …   Wikipedia

• European and Developing Countries Clinical Trials Partnership — The European and Developing Countries Clinical Trials Partnership or EDCTP is a partnership between the European Union (EU), Norway, Switzerland and developing countries and other donors, as well as the pharmaceutical industry, to enable clinical …   Wikipedia

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