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Query: ((DN = "32003L0094" AND DD <= 28/05/2023) OR (RESOURCE_LEGAL_CORRECTS_RESOURCE_LEGAL = "32003L0094" AND DD >= 08/10/2003 AND DD < 28/05/2023 AND (EMBEDDED_ACT_CONSOLIDATED_DATE > 08/10/2003 WHEN EMBEDDED_ACT_CONSOLIDATED_CELEX = "02003L0094*" OR EMBEDDED_ACT_CONSOLIDATED_DATE = NULL)) OR ((RESOURCE_LEGAL_REPEALS_RESOURCE_LEGAL = "32003L0094" OR RESOURCE_LEGAL_IMPLICITLY_REPEALS_RESOURCE_LEGAL = "32003L0094" OR RESOURCE_LEGAL_RENDERS_OBSOLETE_RESOURCE_LEGAL = "32003L0094" OR RESOURCE_LEGAL_REPLACES_RESOURCE_LEGAL = "32003L0094" OR RESOURCE_LEGAL_SUSPENDS_RESOURCE_LEGAL = "32003L0094" OR RESOURCE_LEGAL_PARTIALLY_SUSPENDS_RESOURCE_LEGAL = "32003L0094" OR RESOURCE_LEGAL_AMENDS_RESOURCE_LEGAL = "32003L0094") AND DD > 08/10/2003 AND DD <= 28/05/2023)) AND (EMBEDDED_WHE_EXPRESSION_LG=ENG), Search language: English

Commission Directive (EU) 2017/1572 of 15 September 2017 supplementing Directive 2001/83/EC of the European Parliament and of the Council as regards the principles and guidelines of good manufacturing practice for medicinal products for human use (Text with EEA relevance. )

C/2017/6127

In force

CELEX number:
32017L1572
Form:
Directive
Responsible body:
SANTE
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
15/09/2017; Date of adoption

Commission Directive 2003/94/EC of 8 October 2003 laying down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use and investigational medicinal products for human use (Text with EEA relevance)

No longer in force

CELEX number:
32003L0094
Form:
Directive
Author:
European Commission
Date of document:
08/10/2003