# 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) (revoked)

EU Regulation No 1252/2014 · adopted 28 May 2014

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)

## Introductory text

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) (revoked)
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## 1 Scope

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## 2 Definitions

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## 3 Quality management

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## 4 Personnel

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## 5 Buildings and facilities

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## 6 Equipment

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## 7 Documentation and records

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## 8 Material management

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## 9 Production and in-process control

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## 10 Packaging and labelling

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## 11 Placing on the market

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## 12 Laboratory controls

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## 13 Validation

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## 14 Change control

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## 15 Rejection and returns

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## 16 Complaints and recalls

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## 17 Contract manufacturing

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## 18 Repackaging

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## 19 Entry into force

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## Signature

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Source: https://www.legislation.gov.uk/eur/2014/1252 (the official version)
Page: https://openlegislation.uk/eu-regulation-2014-1252
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.