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Council Regulation (EC) No 111/2005 of 22 December 2004 laying down rules for the monitoring of trade between the Community and third countries in drug precursors article 21 CELEX: 02005R0111-20240603 1. The application for the import authorisations referred to in Article 20 shall contain at least the following: (a) the names and addresses of the importer, the exporter of the third country, any other operator involved and the ultimate consignee; (b) the name of the scheduled substance as stated in the Annex or, in the case of a mixture or a natural product, its name and the eight-digit CN code and the name of any scheduled substance, as stated in the Annex, contained in the mixture or in the natural product; (c) the quantity and weight of the scheduled substance and, in the case of a mixture or a natural product, the quantity, weight, and, if available, the percentage of any scheduled substance contained therein; (d) if available, details of the transport arrangements, such as methods and means of transport, and date and place of envisaged import activities, and (e) the number of the licence or registration referred to in Articles 6 and 7. 2. A decision on the application for an import authorisation shall be taken within a period of 15 working days from the date on which the competent authority considers the file to be complete. |