3. The applications to the Executive referred to in paragraph 2 are—
(a)an application under regulation 7(1) for a variation of the requirements subject to which an active substance is included in Annex I, IA or IB;
(b)an application under regulation 7(2) for the renewal of the inclusion of an active substance in Annex I, IA or IB;
(c)an application under regulation 9 for the authorisation of, or the renewal of an authorisation of, a biocidal product;
(d)an application under regulation 10 for the registration of, or the renewal of the registration of, a biocidal product;
(e)an application under regulation 11(5) for the authorisation of a biocidal product;
(f)an application under regulation 12(5) for the registration of a biocidal product;
(g)an application under regulation 13 for the provisional authorisation of, or the renewal of the provisional authorisation of, a biocidal product;
(h)an application under regulation 14 for the provisional registration of, or the renewal of a provisional authorisation of, a biocidal product;
(i)an application for an authorisation under regulation 17.