Article R5121-132
For pharmaceutical products with a parallel import authorisation, Customs officers check the import authorisation number on the packaging. If this number does not appear on the packaging at the time o…
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Showing 1761–1770 of 6711 articles for “Art. CA Rouen 13 juin 2000 n° 1999/04931”
For pharmaceutical products with a parallel import authorisation, Customs officers check the import authorisation number on the packaging. If this number does not appear on the packaging at the time o…
…the fourth paragraph of Article L. 5124-11 shall be sent to the Agence nationale de sécurité du médicament et des produits de santé by any means capable of providing a date certain by the exporting ph…
…subject to the specific provisions relating to them respectively, which are set out in articles R. 5132-27 and R. 5132-86.
…product, as soon as he is aware of it. It will also inform the Agence nationale de sécurité du médicament et des produits de santé of any changes of which it is aware concerning the marketing authori…
…le R. 5124-2, of a proprietary medicinal product benefiting from a parallel import authorisation is carried out by the holder of this authorisation, provided that he has obtained the authorisation to…
When, in application of the second paragraph of Article L. 5124-11, the Director General of the Agence nationale de sécurité du médicament et des produits de santé intends to prohibit the export of a…
…determined, after consultation with the Director General of the Agence nationale de sécurité du médicament et des produits de santé, by order of the Minister for Health. III -Where a medicinal product…
Any change in the holder of an authorisation to open a pharmaceutical establishment is subject to prior authorisation. However, the Director General of the Agence nationale de sécurité du médicament e…
A schedule of periods for submitting the visa applications referred to in Article L. 5122-9 is set for each year, by decision of the Director General of the National Agency for the Safety of Medicines…
…sing of the medicinal products, products or articles mentioned in article L. 4211-1 and sterile medical devices in the structures authorised to provide care can be ensured at least once a day and with…
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