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Regulation (EC) No 726/2004 Article 42

Article 42

The applicant or the holder of a marketing authorisation shall be responsible for the accuracy of the documents and of the data submitted.

Read the full instrument → · Read this in context: TITLE III — AUTHORISATION AND SUPERVISION OF VETERINARY MEDICINAL PRODUCTS →

Other provisions in TITLE III — AUTHORISATION AND SUPERVISION OF VETERINARY MEDICINAL PRODUCTS

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 42 of Regulation (EC) No 726/2004 (LawPlayer, data as of 2026-07-04)

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