Regulation (EU) No 649/2012 of the European Parliament and of the CouncilShow full title

Article 2 U.K. Scope

1. This Regulation shall apply to:

(a) certain hazardous chemicals that are subject to the prior informed consent procedure under the Convention (the ‘PIC procedure’);

(b) certain hazardous chemicals that are banned or severely restricted within the Union or a Member State;

(c) chemicals when exported in so far as their classification, labelling and packaging are concerned.

2. This Regulation shall not apply to any of the following:

(a) narcotic drugs and psychotropic substances covered by 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(1);

(b) radioactive materials and substances covered by Council Directive 96/29/Euratom of 13 May 1996 laying down basic safety standards for the protection of the health of workers and the general public against the dangers arising from ionizing radiation(2);

(c) wastes covered by Directive 2008/98/EC of the European Parliament and of the Council of 19 November 2008 on waste(3);

(d) chemical weapons covered by Council Regulation (EC) No 428/2009 of 5 May 2009 setting up a Community regime for the control of exports, transfer, brokering and transit of dual-use items(4);

(e) food and food additives covered by Regulation (EC) No 882/2004 of the European Parliament and of the Council of 29 April 2004 on official controls performed to ensure the verification of compliance with feed and food law, animal health and animal welfare rules(5);

(f) feedingstuffs covered by Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety(6), including additives, whether processed, partially processed or unprocessed, intended to be used for oral feeding to animals;

(g) genetically modified organisms covered by Directive 2001/18/EC of the European Parliament and of the Council of 12 March 2001 on the deliberate release into the environment of genetically modified organisms(7);

(h) save to the extent covered by Article 3(5)(b) of this Regulation, proprietary medicinal products and veterinary medicinal products covered by Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use(8) and Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products(9) respectively.

3. This Regulation shall not apply to chemicals exported for the purpose of research or analysis in quantities that are unlikely to affect human health or the environment and that in any event do not exceed 10 kg from each exporter to each importing country per calendar year.

Notwithstanding the first subparagraph, exporters of the chemicals referred to therein shall obtain a special reference identification number using the Database referred to in Article 6(1)(a) and provide that reference identification number in their export declaration.

(1)

OJ L 22, 26.1.2005, p. 1.

(2)

OJ L 159, 29.6.1996, p. 1.

(3)

OJ L 312, 22.11.2008, p. 3.

(4)

OJ L 134, 29.5.2009, p. 1.

(5)

OJ L 165, 30.4.2004, p. 1.

(6)

OJ L 31, 1.2.2002, p. 1.

(7)

OJ L 106, 17.4.2001, p. 1.

(8)

OJ L 311, 28.11.2001, p. 67.

(9)

OJ L 311, 28.11.2001, p. 1.