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Showing 871–880 of 56939 articles for “Art. I-al. 3”
In the event of a change in the classification or maximum residue limit of a pharmacologically active substance in application of Regulation (EC) No 470/2009 of the European Parliament and of the Coun…
…5141-5, any variation or extension, as provided for in Chapter I of Commission Regulation (EC) No 1234/2008 of 28 November 2008 concerning the examination of variations to the terms of a marketing aut…
The marketing authorisation holder submits to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail any proposed amendment to the label…
The marketing authorisation is renewable on application by the holder to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail no later…
…dministration; the Public Prosecutor may bring it as an accessory action to the public prosecution. 3. In proceedings referred to customs officers pursuant to I and II of Article 28-1 of the Code of C…
For health professionals covered by the provisions of article L. 4138-2 of the Defence Code, the Minister for Defence adapts the multi-year continuing professional development programmes proposed by t…
The certificate drawn up by the person responsible for the transfer of the second-hand medical device certifies that it has undergone regular maintenance in accordance with the provisions of article R…
For the purposes of II of Article L. 613-20-4, the Autorité de contrôle prudentiel et de résolution shall draw up and send to the other competent authorities of the Member States of the European Union…
1. Notwithstanding the provisions of
…24-96 and to the texts adopted for its application is punishable by an administrative fine of up to 3,000 euros for a natural person and 15,000 euros for a legal entity. This fine is imposed under the…
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