1.In addition to data to be provided pursuant to Article 5, information shall be provided on:
(a)the identity and characterisation of the additive, including the proposed specifications and analytical data;
(b)where applicable, the particle size, particle size distribution and other physicochemical characteristics;
(c)the manufacturing process;
(d)presence of impurities;
(e)the stability, reaction and fate in foods to which the additive is added;
(f)where applicable, the existing authorisations and risk assessments;
(g)proposed normal and maximum use levels in F1... food categories F2..., or in a newly proposed food category, or in a more specific foodstuff belonging to one of these categories;
(h)a dietary exposure assessment;
(i)the biological and toxicological data.
2.As regards to the biological and toxicological data, referred to in point (i) of paragraph 1, the following core areas shall be covered:
(a)toxicokinetics;
(b)subchronic toxicity;
(c)genotoxicity;
(d)chronic toxicity/carcinogenicity;
(e)reproductive and developmental toxicity.
Textual Amendments
F1Word in Art. 6(1)(g) omiited (1.4.2025) by The Food and Feed (Regulated Products) (Amendment, Revocation, Consequential and Transitional Provision) Regulations 2025 (S.I. 2025/361), regs. 1(2), 10(3)(a) (with reg. 23)
F2Words in Art. 6(1)(g) omitted (1.4.2025) by virtue of The Food and Feed (Regulated Products) (Amendment, Revocation, Consequential and Transitional Provision) Regulations 2025 (S.I. 2025/361), regs. 1(2), 10(3)(b) (with reg. 23)