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Showing 621–630 of 30729 articles for “Art. R 123-52”
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…
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…
After it has been issued, the parallel import authorisation is suspended or withdrawn by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du…
I.- In the event of repackaging, the holder of a parallel import authorisation for a proprietary veterinary medicinal product shall notify the holder of the marketing authorisation for the proprietary…
When the parallel import application concerns a proprietary veterinary medicinal product which has already been the subject of a parallel import authorisation, and the proprietary veterinary medicinal…
The contribution provided for in Article L. 6331-53 is paid by the collection bodies to France Compétences, in accordance with the procedures specified in an agreement concluded respectively with the…
Participating securities issued to subscribers contain the following information: 1° The company name, followed, where applicable, by its acronym; 2° The form of the issuing company; 3° The amount of…
Veterinary medicinal products for which the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail has restricted the conditions of supply t…
The provisions of this sub-section do not apply to the Armed Forces Blood Transfusion Centre, subject to the provisions of articles R. 1222-47, R. 1222-50 and R. 1222-51.
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