Article 611-27
The application for aid must be submitted before the product is marketed to the public.
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Showing 5401–5410 of 13025 articles for “Art. Euronext Harmonised Market Rules — derivatives”
The application for aid must be submitted before the product is marketed to the public.
…ble, and a reference to any appropriate collection system in place; 12° The name and address of the marketing authorisation holder and, where applicable, of the company exploiting the medicinal produc…
…n Article R. 5121-51-1, the Director General of the Agency will notify the States concerned and the marketing authorisation holder of the agreement. In accordance with the assessment report thus appro…
Following the granting of a marketing authorisation, including for an authorisation granted before 21 July 2012, the Director General of the Agence nationale de sécurité du médicament et des produits…
…n of a proprietary medicinal product constitutes a parallel import with a view to placing it on the market in France: 1° Which comes from another Member State of the European Community or party to the…
The marketing authorisation holder shall forward without delay to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail, including duri…
…ere is no suitable or available proprietary medicinal product, including because it is not actually marketed, which has a marketing authorisation, one of the authorisations or a compassionate prescrib…
…ch comply with the standards corresponding to the category to which they belong and which transpose harmonised European standards, the references of which have been published in the Journal officiel d…
The conditions laid down in this sub-section are checked when applications for investment approval and production approval are examined.
To be eligible for financial assistance for production and preparation, production companies must meet the following conditions:1° Be established in France;2° Have chairmen, directors or managers, as…
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