Scope
Article 1
This Regulation lays down the principles and guidelines of good manufacturing practice for active substances for medicinal products for human use, including active substances intended for export.
Commission Delegated Regulation (EU) No 1252/2014 Article 1
Commission Delegated Regulation (EU) No 1252/2014 Article 1
Other provisions in Commission Delegated Regulation (EU) No 1252/2014
- Article 2: Definitions
- Article 3: Quality management
- Article 4: Personnel
- Article 5: Buildings and facilities
- Article 6: Equipment
- Article 7: Documentation and records
- Article 8: Material management
- Article 9: Production and in-process control
- Article 10: Packaging and labelling
- Article 11: Placing on the market
CitationArticle 1 of Commission Delegated Regulation (EU) No 1252/2014 (LawPlayer, data as of 2026-07-04)
© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.
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