Paragraph 3 I1

Northern Ireland Not yet in force

Changes not yet applied. Later legislation changes this provision in ways not yet written into the text below:

Sch. 11 para. 1 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 2 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 3 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 4 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 5 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 6 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 7 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 8 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 9 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 10 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 11 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 12 coming into force by Biocidal Products 2001 reg. 1
Sch. 11 para. 3(ha) inserted by Biocidal Products 2007 reg. 24
Sch. 11 revoked with savings by Biocidal Products (Fees and Charges) 2013 reg. 9(1)

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.

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