Medicinal Products Act. (The Drug Law) - Germany. Medicinal Products Act in the Version Published on 12 December 2005 (Federal Law Gazette ) Part I P. 3394, Last Amended by Article 1 of the Law of 25th May 2011 (Federal Law Gazette I P. 946)
(2011; 145 pages)

Abstract

It is the purpose of the present Act to guarantee, in the interest of furnishing both human beings and animals with a proper supply of medicinal products, safety in respect of the trade in medicinal products, ensuring in particular the quality, efficacy and safety of medicinal products in accordance with the following provisions....

Übersetzung durch den Sprachendienst des Bundesministeriums für Gesundheit.

Translation provided by the Language Service of the Federal Ministry of Health.

Translations of any materials into languages other than German are intended solely as a convenience to the non-German-reading public. If any questions arise related to the accuracy of the information contained in the translation, please refer to the German version of the document which is the official version of the document. Any discrepancies or differences created in the translation are not binding and have no legal effect for compliance or enforcement purposes.

 
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