Diario Oficial de la Unión Europea del 1/3/2023 - Sección Legislación
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Fuente: Diario Oficial de la Unión Europea - Sección Legislación
EN
1.3.2023
Official Journal of the European Union
L 64/1
II
Non-legislative acts
REGULATIONS
COMMISSION DELEGATED REGULATION EU 2023/439
of 16 December 2022
amending the Annex to Regulation EU No 609/2013 of the European Parliament and of the Council to allow the use of nicotinamide riboside chloride as a source of niacin in food for special medical purposes and total diet replacement for weight control Text with EEA relevance
THE EUROPEAN COMMISSION,
Having regard to the Treaty on the Functioning of the European Union, Having regard to Regulation EU No 609/2013 of the European Parliament and of the Council of 12 June 2013 on food intended for infants and young children, food for special medical purposes, and total diet replacement for weight control and repealing Council Directive 92/52/EEC, Commission Directives 96/8/EC, 1999/21/EC, 2006/125/EC
and 2006/141/EC, Directive 2009/39/EC of the European Parliament and of the Council and Commission Regulations EC No 41/2009 and EC No 953/2009 1, and in particular Article 161 thereof, Whereas:
1
The Annex to Regulation EU No 609/2013 establishes a Union list of substances that may be added to one or more of the categories of food referred to in Article 11 of that Regulation.
2
In accordance with Regulation EU 2015/2283 of the European Parliament and of the Council 2, Commission Implementing Regulation EU 2020/16 3 authorised the placing on the market of nicotinamide riboside chloride as a novel food for use in food supplements as defined in Directive 2002/46/EC of the European Parliament and of the Council 4, for the adult population.
3
Following an application for extension of the use of nicotinamide riboside chloride as a novel food to cover also its use for nutritional purposes as a source of niacin, in particular, in food for special medical purposes and total diet replacement for weight control, the Commission requested the European Food Safety Authority the Authority to deliver an opinion on such extension of use in accordance with Regulation EU 2015/2283 and, following the outcome of that assessment, to evaluate in the context of Regulation EU No 609/2013 the safety and bioavailability of that substance when added to the foods in question. On 14 September 2021, the Authority
1 OJ L 181, 29.6.2013, p. 35.
2 Regulation EU 2015/2283 of the European Parliament and of the Council of 25 November 2015 on novel foods, amending Regulation EU No 1169/2011 of the European Parliament and of the Council and repealing Regulation EC No 258/97 of the European Parliament and of the Council and Commission Regulation EC No 1852/2001 OJ L 327, 11.12.2015, p. 1.
3 Commission Implementing Regulation EU 2020/16 of 10 January 2020 authorising the placing on the market of nicotinamide riboside chloride as a novel food under Regulation EU 2015/2283 of the European Parliament and of the Council and amending Commission Implementing Regulation EU 2017/2470 OJ L 7, 13.1.2020, p. 6.
4 Directive 2002/46/EC of the European Parliament and of the Council of 10 June 2002 on the approximation of the laws of the Member States relating to food supplements OJ L 183, 12.7.2002, p. 51.
