The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026
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Change 1
7 Amendment of Commission Delegated Regulation (EU) 2015/1011
(1) Commission Delegated Regulation (EU) 2015/1011 of 24 April 2015 supplementing Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Union and third countries in drug precursors, and repealing Commission Regulation (EC) 1277/2005 is amended as follows. (2) In Article 3 (conditions for granting licences)— (a) omit paragraph 3; (b) in paragraph 7— (i) for “the United Kingdom” substitute “Great Britain”; (ii) after “third countries” insert “or Northern Ireland”. (3) In Article 8 in paragraph 1 after “country of export” insert “or Northern Ireland”. (4) In Article 9 (information required to monitor trade)— (a) in paragraph 3 after “countries of destination” insert “or Northern Ireland”; (b) in paragraph 4 after “to the third country of export” insert “or Northern Ireland”; (c) in paragraph 5 after “the third countries” insert “or Northern Ireland”. (5) In Article 10 (conditions for determining the lists of the countries of destination for exports of scheduled substances of Categories 2 and 3) after “specific countries of destination” insert “which may include Northern Ireland”. (6) In Article 11 (criteria for determining simplified procedures for pre-export notifications)— (a) in paragraph 2— (i) for “the country of export” substitute “Great Britain”; (ii) after “the third country of destination” insert “or Northern Ireland”; (b) in paragraph 3— (i) after “the country of destination” insert “or Northern Ireland”; (ii) omit “or the ‘Multicultural Chemical Reporting Notification’ set out in Annex III of this Regulation”. (7) In Article 12 (criteria for determining simplified procedures for export authorisations)— (a) in paragraph 1— (i) for “the United Kingdom” substitute “Great Britain”; (ii) after “third country of destination” insert “or Northern Ireland”; (b) in paragraph 2 in sub-paragraph (a) after “in the third country” insert “or Northern Ireland”. (8) Omit Annex II (declaration of the operator on the entry of the scheduled substances into the customs territory of the Union). (9) Omit Annex III (form for multilateral chemical reporting notification).
7 Amendment of Commission Delegated Regulation (EU) 2015/1011
(1) Commission Delegated Regulation (EU) 2015/1011 of 24 April 2015 supplementing Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Union and third countries in drug precursors, and repealing Commission Regulation (EC) 1277/2005 is amended as follows. (2) In Article 3 (conditions for granting licences)— (a) omit paragraph 3; (b) in paragraph 7— (i) for “the United Kingdom” substitute “Great Britain”; (ii) after “third countries” insert “or Northern Ireland”. (3) In Article 8 in paragraph 1 after “country of export” insert “or Northern Ireland”. (4) In Article 9 (information required to monitor trade)— (a) in paragraph 3 after “countries of destination” insert “or Northern Ireland”; (b) in paragraph 4 after “to the third country of export” insert “or Northern Ireland”; (c) in paragraph 5 after “the third countries” insert “or Northern Ireland”. (5) In Article 10 (conditions for determining the lists of the countries of destination for exports of scheduled substances of Categories 2 and 3) after “specific countries of destination” insert “which may include Northern Ireland”. (6) In Article 11 (criteria for determining simplified procedures for pre-export notifications)— (a) in paragraph 2— (i) for “the country of export” substitute “Great Britain”; (ii) after “the third country of destination” insert “or Northern Ireland”; (b) in paragraph 3— (i) after “the country of destination” insert “or Northern Ireland”; (ii) omit “or the ‘Multicultural Chemical Reporting Notification’ set out in Annex III of this Regulation”. (7) In Article 12 (criteria for determining simplified procedures for export authorisations)— (a) in paragraph 1— (i) for “the United Kingdom” substitute “Great Britain”; (ii) after “third country of destination” insert “or Northern Ireland”; (b) in paragraph 2 in sub-paragraph (a) after “in the third country” insert “or Northern Ireland”. (8) Omit Annex II (declaration of the operator on the entry of the scheduled substances into the customs territory of the Union). (9) Omit Annex III (form for multilateral chemical reporting notification).
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