# Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC (Text with EEA relevance), Division 31

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

As regards documentation relating to GMP compliance, the following shall apply.

---
Source: https://www.legislation.gov.uk/eur/2014/536/annex/I/division/F/division/31 (the official version)
Page: https://openlegislation.uk/eu-regulation-2014-536/annex-I/division-F/division-31
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.