Directive · EU
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. )
- Identifier
- CELEX 32017L1572
- Status
- in_force
- Adopted
- 15 September 2017
- Published
- 15 September 2017
- Language
- en
- Official source
- https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32017L1572
- Source provider
- eurlex
- Retrieved
- 2026-08-27T22:14:38.468Z
Identifier
- CELEX: 32017L1572 · eurlex
Direct relationships
PoliticalRepo: CELEX 32017L1572
- Identifier matchPROJECTS_FROM
Same CELEX 32017L1572 projected from PoliticalRepo EUR-Lex row 32017L1572.
LegalInstrument → PoliticalRecord · Open related record
- Identifier matchIDENTIFIER_MATCH
Shared official identifier CELEX=32017L1572.
LegalInstrument → PoliticalRecord · Open related record