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)
| Amendments and corrections | |
|---|---|
| February 9, 2025 | Application - Partial application See Art 50 |
| January 1, 2022 | Modified by 32022R0315
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detail |
| October 11, 2021 | Modified by 32021R1686
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detail |
| January 1, 2021 | Modified by 32021R0457
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detail |
| February 9, 2019 | Application - See Art 50 |
| February 29, 2016 | Entry into force - Date pub. +20 See Art 50 |
| Consolidated texts | ||
|---|---|---|
| January 1, 2022 | Modified by 32016R0161 32022R0315 | 02016R0161-20220101 |
| October 11, 2021 | Modified by 32016R0161 32021R1686 | 02016R0161-20211011 |
| January 1, 2021 | Modified by 32016R0161 32021R0457 | 02016R0161-20210101 |
| February 9, 2016 | Date of publication | 32016R0161 |