Regulation (EC) No 726/2004 Article 17

Article 17

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

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Other provisions in TITLE II — AUTHORISATION AND SUPERVISION OF MEDICINAL PRODUCTS FOR HUMAN USE

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CitationArticle 17 of Regulation (EC) No 726/2004 (LawPlayer, data as of 2026-07-04)

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