20. - 23.01.2009
Heidelberg: Certified Regulatory Affairs Manager
Dr. Hiltrud Horn will give an intensive training course on regulatory requirements in Europe and US. You will get detailed insight into all regulatory documents to be prepared during all phases of drug development, for regulatory submissions and in the post-submission phase. You will learn how to organize and plan meetings with Authorities and how to stay compliant.
For more information please visit the following website:
http://www.iir.de/produkt.aspx?pnr=P2100134
(Conference organized by IIR)
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