Article D6362-12-1
The State representative informs the local authority or its public establishment concerned of the referral to the territorial audit chamber.
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Showing 3911–3920 of 61564 articles for “Art. Cass. com. 12 May 2004 · Cass. com. 19 October 1982 · Cass. 3e civ. 4 February 1976 · Cass. 3e civ. 2 June 1982”
The State representative informs the local authority or its public establishment concerned of the referral to the territorial audit chamber.
The State representative informs the local authority or its public establishment concerned of the referral to the territorial audit chamber.
Professionals who have obtained authorisation to practise part of the profession concerned appear on a separate list containing the professional title under which they are authorised to practise and t…
…sécurité du médicament et des produits de santé sends the coordination group referred to in Article 27 of Directive 2001/83/EC of the European Parliament and of the Council a list of medicinal product…
…he list drawn up by the Commission of the European Communities pursuant to Article 16f of Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code re…
The copy of the import authorisation or temporary use authorisation referred to in article L. 5141-10 is presented during the inspection by the customs officers. For imported veterinary medicinal prod…
…within sixty days from the date of receipt of the complete application referred to in Article R. 5141-123-9 . The period mentioned in the previous paragraph is reduced to thirty days for applications…
…re complied with, in particular those relating to possession and supply referred to in Article R. 5141-112, labelling referred to in Articles R. 5141-73 to R. 5141-75, and the package leaflet referred…
When the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail notifies the holder of the parallel import authorisation for a proprietary v…
…holder in the country of origin of any serious adverse reaction, within the meaning of Article R. 5141-92, concerning the imported proprietary medicinal product, as soon as he is aware of it.
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