Regulation 35 I1

For Article 32, substitute—

“Reference laboratory

1

The appropriate authority may F1designate in accordance with Article 100 of Regulation (EU) 2017/625 a reference laboratory to perform the duties and tasks set out in the Annex.

2

Applicants for authorisation of genetically modified food and feed shall contribute to supporting the costs of the duties and tasks of the reference laboratory.

3

The contributions from applicants shall not exceed the costs incurred in carrying out the validation of detection methods.

4

The appropriate authority may prescribe—

(a)

measures for implementing this Article and the Annex; and

(b)

measures designed to amend non-essential elements of this Regulation and adapting the Annex.”.