Fees for parallel trade applications to the Northern Ireland competent authority are in accordance with the following table, and each item is charged cumulatively.

Item	Chargeable item	Fee(£)
(1)Application for a parallel trade permit for other than personal use.	(1)Application for a parallel trade permit for other than personal use.	(1)Application for a parallel trade permit for other than personal use.
(2)Verification that the product to be traded is identical to a product authorised in accordance with Regulation 1107/2009.	(2)Verification that the product to be traded is identical to a product authorised in accordance with Regulation 1107/2009.	(2)Verification that the product to be traded is identical to a product authorised in accordance with Regulation 1107/2009.
1	Preliminary consideration of an application to determine whether the application can proceed further	229
2	Parallel trade applications—
	(a) co-ordination of application for a new product or change to an existing product involving parallel trade[^f01000]	728
	(b) parallel trade verification[^f01001]	208
	(c) parallel trade permit for personal use	156

Fees for application and evaluation of an active substance, safener , synergist or basic substance

Fees for official recognition of a test facility or organisation

Fees for import tolerances

1

Fees chargeable by a Great Britain competent authority for import tolerances are in accordance with the following table.

Item	Category	Fee(£)
A1	Preliminary consideration of an application to determine whether the application can proceed further	229
A2	Co-ordination of applications	1,872
1	Full Human health description⁽¹⁾	16,224
2	Metabolism and residues evaluation⁽²⁾	6,760
3	Residues evaluation⁽³⁾	2,028

Notes

(1) This category is mainly for active substances not currently approved in respect of the part of Great Britain to which the application relates. In certain cases it may also include active substances still being reviewed if toxicological endpoints have not yet been agreed and accepted in respect of that part of Great Britain.

(2) This category is for active substances where toxicological endpoints have already been agreed and accepted in respect of the part of Great Britain to which the application relates, but the residue definition has only been established for crop groups unrelated to the intended use or imported produce.

(3) This category is for active substances where relevant toxicological endpoints and residue definition have already been agreed and accepted in respect of the part of Great Britain to which the application relates.

Fees for multiple import tolerances for the same active substance are calculated on a modular basis with a charge applied for each crop.

Fees for standalone MRL applications

2

Fees chargeable by a Great Britain competent authority for standalone MRL applications are in accordance with the following table.

SCHEDULE 3 — Maximum residue level supplementary information fees chargeable by a Great Britain competent authority

Notes

(1) This category is for an MRL supplementary information requirement to provide additional information on aspects of the data already evaluated or to provide evidence of the commercial availability of standards for MRL compliance.

(2) This category is for an MRL supplementary information requirement to provide an analytical method for MRL compliance.

(3) This category is for an MRL supplementary information requirement to address the toxicological relevance of a metabolite identified in plants or products of animal origin.

(4) This category is for an MRL supplementary information requirement to address plant or livestock metabolism or any other nature of residue study.

(5) This category is for an MRL supplementary information requirement to provide additional residue trials or any other magnitude of residue study including monitoring data.

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The Plant Protection Products (Fees and Charges) Regulations 2011

Functions in Article 74(1) of Regulation 1107/2009: Northern Ireland

Charge for work under the Plant Protection Products (Sustainable Use) Regulations 2012

1A

Fees for application and evaluation of an active substance, safener , synergist or basic substance

Fees for official recognition of a test facility or organisation

Fees related to application for approval of basic substances

Fees for import tolerances

1

Fees for standalone MRL applications

2

SCHEDULE 3 — Maximum residue level supplementary information fees chargeable by a Great Britain competent authority