The following guideline can be ordered through the address listed in the "Source/Publisher"-category. In cases in which you can order through the Internet we have established a hyperlink.

EC/1234/2008 Commission Regulation (EC) No 1234/2008 of 24 November 2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products (Consolidated version : 2.11

Short Title:
EC/1234/2008
Origin/Publisher:

European Commission

Document Type:
Regulation
Content:
examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products

Go back

GMP Conferences by Topics