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Showing 1141–1150 of 33295 articles for “Art. R 623-12”
The competent authority's assessment of the applicant's command of the French language results in a decision that may be appealed to the administrative court with territorial jurisdiction.
Each year, the Director General of the Agence nationale de sécurité du médicament et des produits de santé sends the coordination group referred to in Article 27 of Directive 2001/83/EC of the Europea…
In the event of the dissolution of a société de participations financières de profession libérale de pharmaciens d'officine, a liquidator is chosen from among the members. Under no circumstances may t…
The Regional Committee for Employment, Vocational Training and Guidance adopts its own rules of procedure, which set out the organisation of its work.
The State is represented in court both as plaintiff and defendant by the Director General of the Caisse des dépôts et consignations for all acts relating to the management of the fund mentioned in the…
The application for authorisation to import a proprietary veterinary medicinal product in parallel is accompanied by a dossier comprising :1° For each presentation, a sample of the proprietary medicin…
I. - The veterinary medicinal product for which parallel import authorisation is requested may differ from the veterinary medicinal product which has obtained marketing authorisation in France, provid…
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…
I.-A proprietary veterinary medicinal product may be imported in parallel with a view to being placed on the market in France if it meets the following conditions: 1° It comes from another Member Stat…
An import authorisation is required for each import operation involving veterinary medicinal products which have undergone all stages of manufacture, including packaging. By way of derogation from the…
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