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Commission Regulation (EC) No 1277/2005 (repealed)Show full title
Commission Regulation (EC) No 1277/2005 of 27 July 2005 laying down implementing rules for Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and for Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Community and third countries in drug precursors (Text with EEA relevance) (repealed)
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Changes over time for: Article 17
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Article 17U.K.
For the purposes of Article 8(2) of Regulation (EC) No 273/2004 operators shall inform the competent authorities in a summary form of the quantities of scheduled substances used or supplied and, in the case of supply, of the quantity supplied to each third party.
The first paragraph shall apply to scheduled substances of Category 3, only upon request by the competent authorities.
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