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Showing 2321–2330 of 21929 articles for “Art. CE 12-5-2022 n° 416727”
…package leaflet referred to in Articles R. 5141-76 to R. 5141-78 and, with regard to pharmacovigilance, in Articles R. 5141-77 to R. 5141-78. 5141-73 to R. 5141-75, and the package leaflet mentioned i…
The veterinarian registers the medicinal products referred to in the first paragraph of article R. 5141-126 using any recording system that allows immediate presentation at the request of the control…
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…
…ued, the parallel import authorisation is suspended or withdrawn by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail if the specia…
…oduct in the Member State from which the product originates of the fact that the product will be placed on the market in France when it is marketed. Upon request, it will provide the marketing authori…
The provisions relating to the import and export of veterinary medicinal products apply : 1° to medicinal products classified as narcotics or to which the narcotics regulations apply in whole or in pa…
…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.
I.- Exceptionally, by way of derogation from article R. 6123-87-1, for Corsica and the overseas departments and regions, and when these territories do not have the corresponding surgical oncology care…
…he holder of the authorisation collects and sends to the Regional Health Agency and the National Cancer Institute, on an annual basis, anonymised indicators for monitoring the quality of its healthcar…
For its application to La Réunion and Mayotte, in article R. 6123-27, after the words "infra-regional", the words "Mahorais, common to La Réunion and Mayotte" are added.
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