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Commission Delegated Regulation (EU) No 1252/2014 of 28 May 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council with regard to principles and guidelines of good manufacturing practice for active substances for medicinal products for human use Text with EEA relevance
Commission Delegated Regulation (EU) No 1252/2014 of 28 May 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council with regard to principles and guidelines of good manufacturing practice for active substances for medicinal products for human use Text with EEA relevance
Publication metadata
- Published:
- Corporate author(s): European Commission
- Subject: drug surveillance , marketing standard , medicinal product , mode of production , quality standard , technical specification
- CELEX : 32014R1252
- OJ : JOL_2014_337_R_0001
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