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Commission Implementing Regulation (EU) 2022/140 Article 3

Commission Implementing Regulation (EU) 2022/140 Article 3

Biological products to be included in the Union antigen, vaccine and diagnostic reagent banks for certain category A diseases

Article 3

1.   The Commission shall include in the Union antigen, vaccine and diagnostic reagent banks the biological products listed in column 2 of the table in Annex I (‘the table’) for the category A diseases listed in column 1 of the table. 2.   The Commission shall maintain in the Union antigen, vaccine and diagnostic reagent banks the types and strains of the biological products listed in column 3 of the table and the quantities of biological products listed in column 4 of the table, and take account of the validity period of the biological products indicated in column 5 thereof.

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Other provisions in Commission Implementing Regulation (EU) 2022/140

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationArticle 3 of Commission Implementing Regulation (EU) 2022/140 (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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