Division III.5.5
United Kingdom
The analytical method shall be evaluated for compliance with VICH GL49 and the additional points raised above. In addition, the F1appropriate authority shall consult the F2relevant national reference laboratories for control of residues for the particular substance type on the adequacy of the available methods and validation data.
Annotations
Textual amendments
- F1
Words in Annex 1 para. 3(5) substituted (31.12.2020) by The Veterinary Medicines and Animals and Animal Products (Examination of Residues and Maximum Residue Limits) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/676), regs. 1(2)(b), 10(4)(j)(i); 2020 c. 1, Sch. 5 para. 1(1)
- F2
Words in Annex 1 para. 3(5) substituted (31.12.2020) by The Veterinary Medicines and Animals and Animal Products (Examination of Residues and Maximum Residue Limits) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/676), regs. 1(2)(b), 10(4)(j)(ii); 2020 c. 1, Sch. 5 para. 1(1)