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Commission Delegated Regulation (EU) 2017/1569 of 23 May 2017 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 (Text with EEA relevance)

Chapter III INSPECTIONS

United Kingdom

Original text. Later amendments are not shown.

17Supervision by inspection
18Cooperation and coordination of inspections
19Recognition of inspection conclusions
20Empowerments of the inspectors
21Competence and obligations of the inspectors
22Quality system
23Impartiality of inspectors
24Access to premises
25Suspension or revocation of manufacturing authorisation

Chapter III

Legislation: Commission Delegated Regulation (EU) 2017/1569 of 23 May 2017 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 (Text with EEA relevance)
Citation: EU Regulation 2017/1569, chapter iii
Official version: legislation.gov.uk

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Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives. legislation.gov.uk is the official version.

Not legal advice.

👋 Jason Cartwright