The Biocidal Products (Fees and Charges) Regulations (Northern Ireland) 2015

Type Ni-Statutory-Rule
Publication 2015-05-20
Last updated 2015-07-01
State In force
Jurisdiction Northern Ireland
Department Government Printer for Northern Ireland
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Made: 20th May 2015

Coming into operation: 1st July 2015

The Regulations give effect without modifications to proposals submitted to the Department by the Health and Safety Executive for Northern Ireland under Article 13(1A) of the 1978 Order[^f00007].

Citation and commencement

1

These Regulations may be cited as the Biocidal Products (Fees and Charges) Regulations (Northern Ireland) 2015 and shall come into operation on 1st July 2015.

Interpretation

2

Functions of the Member State

3

The functions of the Member State referred to in Article 80(2) of the Biocides Regulation are to be performed by the Executive.

Fees

4

Revocations and savings provisions

5

SCHEDULE — ACTIVITIES IN RESPECT OF WHICH A FEE IS PAYABLE AND DAILY RATE

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) Work relating to a request for inclusion of an active substance in Annex I on behalf of an economic operator. £447
(e) Meetings with applicants and prospective applicants. £447
(f) Evaluation of an application to authorise a biocidal product under the simplified procedure. £393
(g) Validation of an application for a national authorisation of a biocidal product. £393
(h) Evaluation of an application for a national authorisation of a biocidal product. £393
(i) Evaluation of an application to renew a national authorisation of a biocidal product. £393
(j) Validating, processing and determining an application to mutually recognise a biocidal product in sequence, and subsequent authorisation. £393
(k) Processing and determining an application for mutual recognition in parallel as a concerned Member State. £393
(l) Processing and determining an application for mutual recognition by an official or scientific body. £393
(m) Validating an application for Union Authorisation of a biocidal product. £393
(n) Evaluation of an application for Union Authorisation of a biocidal product £393
(o) Evaluation of an application to renew a Union Authorisation. £393
(p) Determination of an application to amend an existing biocidal product authorisation. £393
(q) Determination of an application for a parallel trade permit. £393
(r) Evaluation of an application for an emergency use permit. £393
(s) Evaluation of an application under Regulation 12 of the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2013. £393

Signed

Sealed with the Official Seal of the Department of Enterprise, Trade and Investment on 20th May 2015.

Jackie Kerr — A senior officer of the — Department of Enterprise, Trade and Investment

Explanatory note

(This note is not part of the Regulations)

EXPLANATORY NOTE

These Regulations provide the charging regime in relation to Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (“the Biocides Regulation”; OJ No L167, 27.06.12, p.1).

The Biocides Regulation replaces Directive 98/8/EC (OJ No. L123, 24.4.98, p.1) of the European Parliament and the Council of 16th February 1998, which laid down harmonised rules for the placing on the market of biocidal products. The Biocides Regulation lays down revised harmonised rules for the approval of active substances and the making available on the market of biocidal products.

Regulation 3 makes provision for the functions of the Member State referred to in Article 80(2) to be performed by the Executive.

Regulation 4 and the Schedule enable the Executive to charge fees, at a daily rate per person, for work carried out within the scope of the Biocides Regulation and the Biocidal Products (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2013. These fees were previously prescribed in the Biocidal Products (Fees and Charges) Regulations (Northern Ireland) 2013. Regulation 4 does not reproduce the annual charge made under those Regulations.

Regulation 5 (1) revokes the Biocidal Products (Fees and Charges) Regulations (Northern Ireland) 2013 subject to Regulation 5 (2).

Regulation 5 (2) sets out those provisions of the Biocidal Products Regulations (Northern Ireland) 2001 which continue to apply for the purposes of calculating the fee payable in respect of the evaluation of applications for biocidal product authorisations submitted before 1 September 2013.

In Great Britain the corresponding legislation is contained within the Health and Safety and Nuclear (Fees) Regulations 2015 (S.I. 2015/363). The Great Britain Health and Safety Executive has prepared an impact assessment of the effect that the Regulations will have on the costs of business and the voluntary sector. Analysis of the removal of the requirement to pay the biocidal products annual charge can be found at paragraphs 22 to 33. A copy of the impact assessment is available from the Health and Safety Executive for Northern Ireland, 83 Ladas Drive, Belfast, BT6 9FR. A copy of the assessment has been annexed to the Explanatory Memorandum, placed in the library of the Northern Ireland Assemblyand is also available alongside these Regulations at www.legislation.gov.uk.

Footnotes

[^f00001]: Formerly the Department of Economic Development; see S.I. 1999/283 (N.I. 1), Article 3(5); that Department was formerly the Department of Manpower Services; see S.I. 1982/846 (N.I.11), Article 3

[^f00002]: S.I. 1981/1536 for the designation in relation to the notification and control of substances and S.I. 1999/2788 in relation to measures relating to biocides

[^f00003]: 1972 c.68

[^f00004]: SeeArticle 2(2) of S.I. 1978/1039 (N.I. 9)

[^f00005]: 1972 c.68; the enabling powers conferred by section 2(2) were extended by virtue of section 1 of the European Economic Area Act 1993 (c.51). Section 2(2) was further amended by section 27(1), and paragraphs 2 and 3 of Schedule 2 by section 27(2), of the Legislative and Regulatory Reform Act 2006 (C .51)

[^f00006]: S.I. 1978/1039 (N.I. 9)

[^f00007]: Article 13(1A) was substituted by S.I. 1998/2795 (N.I. 18), Article 4

[^f00008]: OJ L167 27.06.2012, p.1.

[^f00009]: 1954 c.33 (N.I.)

[^f00010]: S.R. 2013 No. 206

[^f00011]: S.R. 2013 No.207

Editorial notes

[^key-088ec7e720c585932f0a14dbd506ba01]: Reg. 1 in operation at 1.7.2015, see reg. 1

[^key-409a69255102bb3d4ccee156fc8c333d]: Reg. 5 in operation at 1.7.2015, see reg. 1

[^key-2fabd07631f272ed0ce965585204ee6f]: Reg. 2 in operation at 1.7.2015, see reg. 1

[^key-103834c812291f4ca482ca333b08f46b]: Reg. 3 in operation at 1.7.2015, see reg. 1

[^key-4d9d854f7e71389800f82853d656a8fb]: Reg. 4 in operation at 1.7.2015, see reg. 1

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