# 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), Annex: Correlation table

Extent: E+W+S+N.I.

Directive 2003/94/EC
This Directive
Commission Delegated Regulation (EU) 2017/1569 supplementing Regulation (EU) No 536/2014 of the European Parliament and of the Council by specifying principles of and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections
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Article 1
Article 1
Article 2
Article 2
Article 2
Article 3
Article 3
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Article 4
Article 4
Article 3
Article 5
Article 5
Article 4
Article 6
Article 6
Article 5(1)
Article 7
Article 7
Article 6
Article 8
Article 8
Article 7
Article 9
Article 9
Article 8
Article 10
Article 10
Article 9
Article 11
Article 11
Article 10
Article 12
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Article 14
Article 15
Article 15
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Article 16
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Article 17
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Article 18
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Article 19
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Source: https://www.legislation.gov.uk/eudr/2017/1572/annex (the official version)
Page: https://openlegislation.uk/eu-directive-2017-1572/annex
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.