Please use this identifier to cite or link to this item: 192.168.6.56/handle/123456789/3108
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dc.contributor.authorFernand Saueren
dc.contributor.editorCrommelin, Daan J.A.-
dc.date.accessioned2018-09-20T08:41:25Z-
dc.date.available2018-09-20T08:41:25Z-
dc.date.issued2013-
dc.identifier.isbn978-1-4614-5949-1-
dc.identifier.urihttp://10.6.20.12:80/handle/123456789/3108-
dc.descriptionA s an initiator and cofounder of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human use, I am pleased to see that this famous “ICH” initiative is still alive and well. I had the privilege of participating directly in this unique process until 2000, as a representative of the European Commission and later as the fi r st director of the European Medicines Agency (EMA).en
dc.languageen-
dc.language.isoenen_US
dc.publisherSpringer New York Heidelbergen_US
dc.subjectmicobiologyen_US
dc.titleGlobal Approach in Safety Testingen_US
dc.typeBooken_US
Appears in Collections:Veterinary Medicine

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