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)
Modified by
Commission Delegated Regulation (EU) 2022/315 of 17 December 2021 amending Delegated Regulation (EU) 2016/161 as regards the derogation from the obligation of wholesalers to decommission the unique identifier of medicinal products exported to the United Kingdom (Text with EEA relevance)
| January 1, 2022 | article 26 paragraph 4 | Addition |
| January 1, 2022 | article 3 paragraph 2 point (d) | Replacement |
| January 1, 2022 | article 36 point (p) | Addition |
| January 1, 2022 | article 20 | Replacement |
| January 1, 2022 | article 32 paragraph 1 point (b) sentence | Addition |
| January 1, 2022 | article 22 unnumbered paragraph | Replacement |