Article 1
Open ↗The Annex to Implementing Regulation (EU) 2021/17 is amended in accordance with the Annex to this Regulation.
Source
Commission Implementing Regulation (EU) 2024/916 of 26 March 2024 amending Implementing Regulation (EU) 2021/17 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council
Commission Implementing Regulation (EU) 2024/916 of 26 March 2024 amending Implementing Regulation (EU) 2021/17 establishing a list of variations not requiring assessment in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council
Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
Article 2
Open ↗This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
Supplementary provisions
ANNEXSupplementary provisions
Open ↗ANNEX In the Annex to Implementing Regulation (EU) 2021/17, part C, entry 10, the following points are added: Variation Requirements The requirements indicated in the line for the main section are valid for each sub-section of the given section. Any additional requirement specified in the sub-section should be read together with the requirements indicated in the main section. Number Conditions Documents to be provided ‘d) — replacement of information on the immediate or outer packaging by an abbreviation or pictogram — replacement of an existing abbreviation or pictogram on the immediate or outer packaging that is not compliant with Commission Implementing Regulation (EU) 2024/875 by another abbreviation or pictogram The new abbreviation or pictogram is included in Annex I or Annex II to Commission Implementing Regulation (EU) 2024/875 adopting a list of abbreviations and pictograms common throughout the Union to be used on the packaging of veterinary medicinal products for the purposes of Article 10(2) and Article 11(3) of Regulation (EU) 2019/6 of the European Parliament and of the Council (OJ L, 2024/875, 22.3.2024, ELI: http://data.europa.eu/eli/reg_impl/2024/875/oj). The addition does not have a negative impact on the readability of the labelling. e) Alignment of the labelling of the immediate packaging with the requirements laid down in Article 12 of Regulation (EU) 2019/6 The packaging qualifies as a small immediate packaging unit under Commission Implementing Regulation (EU) 2024/878 adopting uniform rules on the size of small immediate packaging units of veterinary medicinal products as referred to in Article 12 of Regulation (EU) 2019/6 of the European Parliament and of the Council (OJ L, 2024/878, 22.3.2024, ELI: http://data.europa.eu/eli/reg_impl/2024/878/oj).’
Other acts of the same type
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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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