# Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use (Text with EEA relevance) (revoked), Chapter VIII: OBLIGATIONS OF MARKETING AUTHORISATION HOLDERS, PARALLEL IMPORTERS AND PARALLEL DISTRIBUTORS

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Status: repealed



---
Source: https://www.legislation.gov.uk/eur/2016/161/chapter/VIII (the official version)
Page: https://openlegislation.uk/eu-regulation-2016-161/chapter-VIII
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.