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                                       Details for article 3 of 18 found articles
 
 
  Angleichung der regulatorischen Anforderungen für die klinische Prüfung von Arzneimitteln am Menschen in der EU - Harmonisation of regulatory requirements for clinical trials on medicinal products for human use in the Directive 2001/20/EC and complementary guidance. Implementation of the 12th Law Amending the German Drug Law
 
 
Title: Angleichung der regulatorischen Anforderungen für die klinische Prüfung von Arzneimitteln am Menschen in der EU - Harmonisation of regulatory requirements for clinical trials on medicinal products for human use in the Directive 2001/20/EC and complementary guidance. Implementation of the 12th Law Amending the German Drug Law
Author: Geisler, I.
Hofmann, H.-P.
Nickel, L.
Appeared in: Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
Paging: Volume 48 (2005) nr. 2 pages 141-146
Year: 2005
Contents:
Publisher: Springer-Verlag, Berlin/Heidelberg
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 3 of 18 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands