Article R1342-15
The declaration provided for in Article R. 1342-13 includes the following information:1° The existing name or names of the mixture in question ;2° The qualitative and quantitative composition of the m…
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Showing 8271–8280 of 38229 articles for “Art. R 134-6”
The declaration provided for in Article R. 1342-13 includes the following information:1° The existing name or names of the mixture in question ;2° The qualitative and quantitative composition of the m…
The provisions of this section apply to Saint-Pierre-et-Miquelon under the conditions set out in Article R. 4112-6-1.
For the application of article R. 49-8-2 in New Caledonia, the words: "to the representative of the State in the department in which it has its headquarters and, in Paris, to the Prefect of Police" ar…
The deliberations of the Board of Directors relating to the objects mentioned in 6°, 7°, 8°, 10°, 11° and 16° of article R. 823-7 are enforceable only after they have been approved by the Minister for…
Withdrawal of the approval of the practitioner referred to in article R. 1131-6 is incurred in the event of a breach of the prescriptions provided for in this chapter or in the event of a breach of th…
Tissues or their derivatives or cell therapy preparations are distributed under the responsibility of the responsible person referred to in Article R. 1243-12 or, where applicable, the person responsi…
I. - Subject to the adaptations provided for in II, the provisions of the articles mentioned in the left-hand column of the table below shall apply in New Caledonia, in the wording indicated in the ri…
I. - Subject to the adaptations provided for in II, the provisions of the articles mentioned in the left-hand column of the table below shall apply in French Polynesia, in the wording indicated in the…
The leave due under 1° of article R. 6152-358 may not be carried over to the following year, unless exceptional authorisation is granted by the director of the establishment after consulting the head…
Any change in the marketing authorisation holder is subject to authorisation from the Director General of the Agence nationale de sécurité du médicament et des produits de santé.The application must i…
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