OpenLegislation

Division 2.4.2.2

United Kingdom

Original text. Later amendments are not shown.

Prior to evaluating the residue levels in the reported trials or in products of animal origin F1competent authorities shall examine the following information:

  • data on the proposed good agricultural practice, including data on application as provided for in the Annex to Regulation (EU) No 545/2011 and proposed pre-harvest intervals for envisaged uses, or withholding periods or storage periods, in the case of post-harvest uses,

  • nature of the preparation,

  • analytical methods and the residue definition.

Annotations

Textual amendments

F1

Words in Annex Pt. 1.B points 2.4.2.2, 2.4.2.3 substituted (31.12.2020) by The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), regs. 1(1), 18(8)(b)(x); 2020 c. 1, Sch. 5 para. 1(1)

Notes on Annex

Textual amendments

F1

Words in Annex heading substituted (31.12.2020) by The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), regs. 1(1), 18(7); 2020 c. 1, Sch. 5 para. 1(1)

Notes on Division 2

Textual amendments

F1

Words in Annex Pt. 1.B Section 2 substituted (31.12.2020) by The Plant Protection Products (Miscellaneous Amendments) (EU Exit) Regulations 2019 (S.I. 2019/556), regs. 1(1), 18(8)(b)(ii); 2020 c. 1, Sch. 5 para. 1(1)