X1CHAPTER ISUBJECT MATTER, SCOPE AND DEFINITIONS
Article 2 Definitions
1.
For the purposes of this Regulation:
(a)
(b)
the definition of ‘ food supplement ’ set out in Directive 2002/46/EC shall apply;
(c)
the definitions of ‘nutrition labelling’, ‘protein’, ‘carbohydrate’, ‘sugars’, ‘fat’, ‘saturates’, ‘mono-unsaturates’, ‘poly-unsaturates’, ‘fibre’ set out in F1Annex I to Regulation (EU) 1169/2011 shall apply;
(d)
the definition of ‘ labelling ’ set out in F2Article 2(1)(j) of Regulation (EU) 1169/2011 shall apply.
2.
The following definitions shall also apply:
(1)
‘claim’ means any message or representation, which is not mandatory under F3any enactment, including pictorial, graphic or symbolic representation, in any form, which states, suggests or implies that a food has particular characteristics;
(2)
‘nutrient’ means protein, carbohydrate, fat, fibre, sodium, vitamins and minerals listed in F4Annex I to Regulation (EU) 1169/2011, and substances which belong to or are components of one of those categories;
(3)
‘other substance’ means a substance other than a nutrient that has a nutritional or physiological effect;
(4)
‘nutrition claim’ means any claim which states, suggests or implies that a food has particular beneficial nutritional properties due to:
(a)
the energy (calorific value) it
(i)
provides;
(ii)
provides at a reduced or increased rate; or
(iii)
does not provide; and/or
(b)
the nutrients or other substances it
(i)
contains;
(ii)
contains in reduced or increased proportions; or
(iii)
does not contain;
(5)
‘health claim’ means any claim that states, suggests or implies that a relationship exists between a food category, a food or one of its constituents and health;
(6)
‘reduction of disease risk claim’ means any health claim that states, suggests or implies that the consumption of a food category, a food or one of its constituents significantly reduces a risk factor in the development of a human disease;
F5(7)
‘expert committee’ means a committee with appropriate expertise in the matter to be considered, approved by an appropriate authority to give advice for the purposes of this Regulation;
F6(8)
‘appropriate authority’, subject to point 9, means:
(a)
for regulations, guidelines, applications or the register of claims in relation to England, the Secretary of State;
(b)
for regulations, guidelines, applications or the register of claims in relation to Scotland, the Scottish Ministers;
(c)
for regulations, guidelines, applications or the register of claims in relation to Wales, the Welsh Ministers;
(9)
The appropriate authority is the Secretary of State if consent is given by:
(a)
for regulations, guidelines, applications or the register of claims in relation to Scotland, the Scottish Ministers;
(b)
for regulations, guidelines, applications or the register of claims in relation to Wales, the Welsh Ministers;
(10)
‘relevant authorities’ means the Secretary of State, the Scottish Ministers and the Welsh Ministers;
(11)
‘enactment’ includes any enactment of the types specified in the definition of ‘enactment’ in section 20(1) of the European Union (Withdrawal) Act 2018.