art_42__para — Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31… · Lexiara

art_42__para

Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance) · European Union

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

← Article 42 · All articles · Article 43 →

Source: EUR-Lex (Cellar) · retrieved 2026-11-03 · Text as adopted (Official Journal); later amendments are not incorporated in this text.