Commission Implementing Regulation (EU) 2019/533 of 28 March 2019 concerning a coordinated multiannual control programme of the Union for 2020, 2021 and 2022 to ensure compliance with maximum residue levels of pesticides and to assess the consumer exposure to pesticide residues in and on food of plant and animal origin (Text with EEA relevance) (revoked)
EU Regulation 2019/533 · Adopted 28 March 2019 · Extends to United Kingdom
Commission Implementing Regulation (EU) 2019/533
of 28 March 2019
concerning a coordinated multiannual control programme of the Union for 2020, 2021 and 2022 to ensure compliance with maximum residue levels of pesticides and to assess the consumer exposure to pesticide residues in and on food of plant and animal origin
(Text with EEA relevance) (revoked)
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Annotations to the whole text
Textual amendments
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Regulation revoked (1.1.2024) by Retained EU Law (Revocation and Reform) Act 2023 (c. 28), ss. 1(1), 22(3), Sch. 1 Pt. 2 (with s. 1(3)(4)); S.I. 2023/1363, reg. 2
Contents
- 1Article 1 Repealed
- 2Article 2 Repealed
- 3Article 3 Repealed
- 4Article 4 Repealed
- 5Article 5 Repealed
- Signature
- Annex IAnnex I Repealed
- Annex II: Number of samples referred to in Article 1 Repealed
- (1)Division (1) Repealed
- (2)In addition to the samples required in accordance with point (1), in 2020 the competent authorities must collectively take and analyse five samples of infant formulae and five samples of follow-on formulae. Repealed
- (3)Division (3) Repealed
- (4)Competent authorities using multi-residue methods may use qualitative screening methods on up to 15 % of the samples to be taken and analysed in accordance with point (1). Where a competent authority uses qualitative screening methods, it shall analyse the remaining number of samples by quantitative multi-residue methods. Repealed
- (4A)Division (4A) Repealed
- (5)... Repealed
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Signature
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Annex IF1
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(1)F1
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(2)In addition to the samples required in accordance with point (1), in 2020 the competent authorities must collectively take and analyse five samples of infant formulae and five samples of follow-on formulae.F1
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(3)F1
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(4)Competent authorities using multi-residue methods may use qualitative screening methods on up to 15 % of the samples to be taken and analysed in accordance with point (1). Where a competent authority uses qualitative screening methods, it shall analyse the remaining number of samples by quantitative multi-residue methods.F1
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(5)...F1
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