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Showing 6231–6240 of 69703 articles for “Art. I and II”
When the marketing authorisation for the proprietary medicinal product that has been granted a marketing authorisation in France is amended by the Director General of the Agence nationale de sécurité…
For each parallel import operation, the authorisation holder notifies the Director General of the Agence nationale de sécurité du médicament et des produits de santé of the batch numbers of the author…
The proprietary medicinal product benefiting from a parallel import authorisation is subject to the provisions of the marketing authorisation for the proprietary medicinal product which obtained the m…
I.- Articles R. 5121-133 to R. 5121-135 do not apply to gene therapy and xenogenic cell therapy preparations. II-Any gene therapy or xenogenic cell therapy preparation that does not have the authorisa…
The operation, as defined in the second paragraph of 3° of Article R. 5124-2, of a proprietary medicinal product benefiting from a parallel import authorisation is carried out by the holder of this au…
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…
The authors must have proven artistic experience or training. If there is more than one author, at least one of them must provide proof of this artistic experience or training.
The beneficiary of a writing grant has five months from the date of the decision to award the grant to submit the developed version of the project to the Centre national du cinéma et de l'image animée…
The beneficiary of a concept grant has three months from the date of the decision to award the grant to submit the formalised version of the project to the Centre national du cinéma et de l'image anim…
To be eligible for creative support, authors must be French nationals or equivalent.
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