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The Veterinary Medicines Regulations 2013
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- UK Statutory Instruments
- 2013 No. 2033
- SCHEDULE 5
- Paragraph 22
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Sampling and analysisE+W+S
This section has no associated Explanatory Memorandum
22.—(1) If any enforcement action is taken under this Schedule based on a sample, that sample must have been taken and analysed in accordance with [F1Regulation (EC) No 152/2009 laying down methods of sampling and analysis for the official control of feedingstuffs.]
(2) Unless otherwise specified in the marketing authorisation, it is a defence if the active ingredient in the medicated feedingstuff sample is within the following tolerances—
[F2Tolerance table for medicated feedingstuff
| Level of active ingredient specified on the label | Tolerance |
|---|---|
| ≤500mg/kg | ±30% |
| ˃500mg/kg ≤5g/kg | ±20% |
| ˃5g/kg | ±10%] |
(3) Unless otherwise specified in the Commission Regulation authorising the specified feed additive in question, it is a defence if the active ingredient of a specified feed additive in a feedingstuff sample is within the tolerances set out in Articles 11(5) and paragraph 2(e) of Annex IV to Regulation (EC) No 767/2009 of the European Parliament and of the Council.
Extent Information
E1This version of this provision extends to England and Wales and Scotland only; a separate version has been created for Northern Ireland only
Textual Amendments
F1Words in Sch. 5 para. 22(1) substituted (26.3.2019) 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)(a), 2(4)(e)
F2Sch. 5 para. 22(2) Table substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 143 (with reg. 207)
Sampling and analysisN.I.
22.—(1) If any enforcement action is taken under this Schedule based on a sample, that sample must have been taken and analysed in accordance with [F3Regulation (EC) No 152/2009 laying down methods of sampling and analysis for the official control of feedingstuffs.]
(2) Unless otherwise specified in the marketing authorisation, it is a defence if the active ingredient in the medicated feedingstuff sample is within the following tolerances—
Tolerance table for medicated feedingstuff
| Level of active ingredient specified on the label | Tolerance |
|---|---|
| ≤50 mg/kg | ± 50% |
| >50 mg/kg ≤ 500 mg/kg | ± 40% |
| >500 mg/kg ≤ 5g/kg | ± 30% |
| >5g/kg ≤50g/kg | ± 20% |
| >50g/kg | ± 10% |
(3) Unless otherwise specified in the Commission Regulation authorising the specified feed additive in question, it is a defence if the active ingredient of a specified feed additive in a feedingstuff sample is within the tolerances set out in Articles 11(5) and paragraph 2(e) of Annex IV to Regulation (EC) No 767/2009 of the European Parliament and of the Council.
Extent Information
E2This version of this provision extends to Northern Ireland only; a separate version has been created for England and Wales and Scotland only
Textual Amendments
F3Words in Sch. 5 para. 22(1) substituted (26.3.2019) 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)(a), 2(4)(e)
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