Article R158
In all cases where the documents of a proceeding are sent, the court clerk is required to attach an inventory, which he shall draw up free of charge, as prescribed in article 586.
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Showing 9641–9650 of 21091 articles for “Art. CA Paris 20-5-2009 n° 08-2432”
In all cases where the documents of a proceeding are sent, the court clerk is required to attach an inventory, which he shall draw up free of charge, as prescribed in article 586.
Articles R. 741-11 relating to the rectification of material errors, R. 741-12 relating to the fine for abusive recourse, R. 742-2, with the exception of the last paragraph, and R. 742-4 to R. 742-6 r…
…e on which the penalty is to take effect, taking into account the time limit for appeal and, in the case of the national disciplinary chamber, where applicable, the time limit for lodging an objection…
…latory provisions to which it applies. The decision shall state that the rapporteur and, where applicable, the parties, the persons who represented or assisted them and any person summoned to the hear…
Where an application for marketing authorisation in France is made for a medicinal product which has already been authorised or is the subject of an application for marketing authorisation currently b…
The applicant is responsible for the accuracy and truthfulness of the documents and data supplied to the Agency when the application for marketing authorisation is submitted and during its examination…
Where the application for marketing authorisation concerns a generator, it shall also include: 1° A general description of the system and a detailed description of the components of the system likely…
The application for marketing authorisation is sent to the Director General of the Agence nationale de sécurité du médicament et des produits de santé. It must state : 1° The name and address of the f…
The application provided for in Article R. 5121-21 must be accompanied by a dossier containing the following information and documents, updated as necessary, presented in accordance with the order ref…
When an application for authorisation concerns a generic medicinal product of a reference medicinal product which has not been authorised in France, the applicant must indicate the Member State of the…
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