European Agency for the Evaluation of Medicinal Products.
Agence européenne pour l'évaluation des médicaments
European Medicines Agency European Union agency in charge of being the highest authority in the field of medicines regulation
Agence européenne des médicaments
Agencia Europea para la Evaluación de Medicamentos
欧州医薬品審査庁
Evropská agentura pro léčivé přípravky
VIAF ID: 135204604 ( Corporate )
Permalink: http://viaf.org/viaf/135204604
Preferred Forms
- 110 2 _ ‡a Agence européenne des médicaments
- 210 | | ‡a Agence européenne pour l'évaluation des médicaments
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- 110 2 _ ‡a Agence européenne pour l'évaluation des médicaments
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- 110 2 0 ‡a Agencia Europea para la Evaluación de Medicamentos
- 110 2 _ ‡a European Agency for the Evaluation of Medicinal Products
- 110 2 _ ‡a European Agency for the Evaluation of Medicinal Products
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- 110 2 _ ‡a European Agency for the Evaluation of Medicinal Products
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- 110 2 _ ‡a European Medicines Agency ‡c European Union agency in charge of being the highest authority in the field of medicines regulation
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- 110 2 _ ‡a 欧州医薬品審査庁
4xx's: Alternate Name Forms (100)
5xx's: Related Names (3)
Works
Title | Sources |
---|---|
Allg. Tatigk.ber. eur. Agent. Beurteil. Arzneim. | |
Annuaire | |
Annual report of the European Medicines Agency ... | |
Arbeitsprogramm der Europäischen Agentur für die Beurteilung von Arzneimitteln. | |
Biological standardization and control, c1997: | |
camán searraigh (luibh) | |
Directory ... | |
EMEA annual report for ... | |
EMEA-Jahresbericht ... | |
Erdrauchkraut | |
European public assessment reports [for veterinary medicines] | |
Fumariae herba | |
fumdeterra | |
fumitory (herb) | |
Gonal-F®, 1996 | |
Informe anual EMEA ... | |
Laba klīniskā prakse | |
Latvijas Vēstnesis, Nr.69 (2004, 1.maijs), A92.,ISSN 1407-0391: | |
Note for guidance on plasma-derived medicinal products | |
PDA/EMEA European virus safety forum Paul-Ehrlich-Institut, Langen, Germany, september 29-october 1, 2003 proceedings of a conference organized by the PDA, and the European agency for the evaluation of medicinal products (EMEA) | |
Programa de trabajo de la Agencia Europea para la Evaluación de Medicamentos | |
Rapp. gén. act. Agence eur. éval. médicam. | |
Rapport annuel EMEA pour ... | |
Rapport d'évaluation public européen | |
Résumé du programme de travail de l'Agence européenne des médicaments .. | |
Sixth General Report : 2000 | |
Starptautiskās harmonizācijas konferences (SHK) (5. posms)/Patentēto medicīnisko produktu komiteja (PMPK) (ICH/CPMP/135/95) : norādījumi par labu klīnisko praksi = Guideline for good clinical practice : IGH (Step 5)/CPMP : (CPMP/IHC/135/95). Pasaules Medicīnas asociācijas Helsinku deklarācija. | |
Uirusu baridēshon shiken ni kansuru gaidansu = Note for guidance on virus validation studies : Uirusu fukatsuka oyobi jokyo no yūkōsei o hyōkasuru shiken no sekkei kiyo oyobi kaishaku ; Kesshō yurai iyakuhin ni kansuru gaidansu. | |
Work programme ... | |
ウイルス・バリデーション試験に関するガイダンス = Note for guidance on virus validation studies : ウイルス不活化および除去の有効性を評価する試験の設計、寄与および解釈 |