# The Human Medicines Regulations 2012, Paragraph 14

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

A standardised text relating to adverse event reporting in accordance with the third sub-paragraph of Article 59(1) of the 2001 Directive.

---
Source: https://www.legislation.gov.uk/uksi/2012/1916/schedule/27/paragraph/14 (the official version)
Page: https://openlegislation.uk/human-medicines-regulations-2012/schedule-27/paragraph-14
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.