dc.contributor.author | Fernand Sauer | en |
dc.contributor.editor | Crommelin, Daan J.A. | |
dc.date.accessioned | 2018-09-20T08:41:25Z | |
dc.date.accessioned | 2023-07-20T09:13:34Z | |
dc.date.available | 2018-09-20T08:41:25Z | |
dc.date.available | 2023-07-20T09:13:34Z | |
dc.date.issued | 2013 | |
dc.identifier.isbn | 978-1-4614-5949-1 | |
dc.identifier.uri | http://10.215.13.25/handle/123456789/3108 | |
dc.description | A 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.language | en | |
dc.language.iso | en | en_US |
dc.publisher | Springer New York Heidelberg | en_US |
dc.subject | micobiology | en_US |
dc.title | Global Approach in Safety Testing | en_US |
dc.type | Book | en_US |