• “Regulation 354/2013” means Commission Implementing Regulation (EU) No 354/2013 of 18 April 2013 on changes of biocidal products authorised in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council;

• “Regulation 1062/2014” means Commission Delegated Regulation (EU) No 1062/2014 of 4 August 2014 on the work programme for the systematic examination of all existing active substances contained in biocidal products referred to in Regulation (EU) No 528/2012 of the European Parliament and of the Council.

1

The Executive shall charge fees for—

a

work it carries out within the scope of the Biocides Regulation which relates to the activities listed in column 1 of the Table in the Schedule;

b

work it carries out in order to evaluate an application for a change to an authorised product under Regulation 354/2013;

c

work it carries out in order to determine an application to be a participant for the review of an active substance/product-type combination under Article 17 of Regulation 1062/2014; and

d

work it carries out in order to evaluate an application under regulation 12 of the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 201336.

Table

1 Activity	2 Fee per person per day worked
(a) Validation of an application for approval of an active substance	£447
(b) Evaluation of an application to approve an active substance	£447
(c) Evaluation of an application to renew an active substance approval	£447
(d) Validation of an application to amend the conditions of approval of an active substance	£447
(e) Evaluation of an application to amend the conditions of approval of an active substance	£447
(f) Work relating to a request for inclusion of an active substance in the Simplified Active Substance List made on behalf of an economic operator	£447
(g) Validation of an application to amend the conditions of inclusion of an active substance in the Simplified Active Substance List	£447
(h) Evaluation of an application to amend the conditions of inclusion of an active substance in the Simplified Active Substance List	£447
(i) Meetings with applicants and prospective applicants	£447
(j) Evaluation of an application to authorise a biocidal product under the simplified procedure	£393
(k) Validation of an application for a national authorisation of a biocidal product	£393
(l) Evaluation of an application for a national authorisation of a biocidal product	£393
(m) Evaluation of an application to renew a national authorisation of a biocidal product	£393
(n) Determination of an application to amend an existing biocidal product authorisation	£393
(o) Evaluation of an application for an emergency use permit	£393
(p) Assessment of an application to be included in the list of suppliers maintained under Article 95 of Regulation 528/2012	£447
(q) Determination of a request that information on an active substance or product is not made publicly available	£447
(r) Determination of the classification of a proposed change to an authorised product in accordance with Regulation 354/2013	£393
(s) Determination of an application to be a participant for the review of an active substance/product-type combination under Article 17 of Regulation 1062/2014	£447
(t) Assessment of technical equivalence	£447
(u) Evaluation of an application under regulation 12 of the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2013	£393