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Query: ((BF = "31993R2309" AND DD = 01/10/2003) OR (RESOURCE_LEGAL_CORRECTS_RESOURCE_LEGAL = "31993R2309" AND DD >= 01/10/2003 AND DD < 07/02/2023 AND (EMBEDDED_ACT_CONSOLIDATED_DATE > 01/10/2003 OR EMBEDDED_ACT_CONSOLIDATED_DATE = NULL)) OR ((RESOURCE_LEGAL_REPEALS_RESOURCE_LEGAL = "31993R2309" OR RESOURCE_LEGAL_IMPLICITLY_REPEALS_RESOURCE_LEGAL = "31993R2309" OR RESOURCE_LEGAL_RENDERS_OBSOLETE_RESOURCE_LEGAL = "31993R2309" OR RESOURCE_LEGAL_REPLACES_RESOURCE_LEGAL = "31993R2309" OR RESOURCE_LEGAL_SUSPENDS_RESOURCE_LEGAL = "31993R2309" OR RESOURCE_LEGAL_PARTIALLY_SUSPENDS_RESOURCE_LEGAL = "31993R2309" OR RESOURCE_LEGAL_AMENDS_RESOURCE_LEGAL = "31993R2309") AND DD > 01/10/2003 AND DD <= 07/02/2023)) AND (EMBEDDED_WHE_EXPRESSION_LG=ENG), Search language: English

Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)

In force

CELEX number:
32004R0726
Form:
Regulation
Author:
European Parliament, Council of the European Union
Date of document:
31/03/2004