OpenLegislation

Commission Regulation (EU) No 252/2012 of 21 March 2012 laying down methods of sampling and analysis for the official control of levels of dioxins, dioxin-like PCBs and non-dioxin-like PCBs in certain foodstuffs and repealing Regulation (EC) No 1883/2006 (Text with EEA relevance) (repealed)

EU Regulation No 252/2012 · Adopted 21 March 2012 · Extends to United Kingdom

Original text. legislation.gov.uk does not revise this item, so later amendments are not shown here. Changes made to it are listed under each provision when known.

Commission Regulation (EU) No 252/2012

of 21 March 2012

laying down methods of sampling and analysis for the official control of levels of dioxins, dioxin-like PCBs and non-dioxin-like PCBs in certain foodstuffs and repealing Regulation (EC) No 1883/2006

(Text with EEA relevance) (repealed)

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Annotations to the whole text

Textual amendments

F1

Repealed by Commission Regulation (EU) No 589/2014 of 2 June 2014 laying down methods of sampling and analysis for the control of levels of dioxins, dioxin-like PCBs and non-dioxin-like PCBs in certain foodstuffs and repealing Regulation (EU) No 252/2012 Text with EEA relevance.

Contents

  1. 1Article 1 Repealed
  2. 2Article 2 Repealed
  3. 3Article 3 Repealed
  4. 4Article 4 Repealed
  5. 5Article 5 Repealed
  6. 6Article 6 Repealed
  7. Signature
  8. Annex I: Definitions and abbreviations Repealed
  9. IDEFINITIONS Repealed
  10. IIABBREVIATIONS USED Repealed
  11. Annex II: Methods of sampling for offical control of levels of dioxins (PCDD/PCDF), dioxin-like PCBs and non-dioxin-like PCBs in certain foodstuffs Repealed
  12. ISCOPE Repealed
  13. GENERAL PROVISIONS Repealed
  14. 1Personnel Repealed
  15. 2Material to be sampled Repealed
  16. 3Precautions to be taken Repealed
  17. 4Incremental samples Repealed
  18. 5Preparation of the aggregate sample Repealed
  19. 6Replicate samples Repealed
  20. 7Packaging and transmission of samples Repealed
  21. 8Sealing and labelling of samples Repealed
  22. IIISAMPLING PLAN Repealed
  23. 1Division of lots into sublots Repealed
  24. 2Number of incremental samples Repealed
  25. 3Specific provisions for the sampling of lots containing whole fishes of comparable size and weight Repealed
  26. 4Sampling of lots of fish containing whole fishes of different size and/or weight Repealed
  27. 5Sampling at retail stage Repealed
  28. COMPLIANCE OF THE LOT OR SUBLOT WITH THE SPECIFICATION Repealed
  29. 1As regards non-dioxin-like PCBs Repealed
  30. 2As regards dioxins (PCDD/PCDF) and dioxin-like PCBs Repealed
  31. VEXCEEDANCE OF ACTION LEVELS Repealed
  32. Annex III: Sample preparation and requirements for methods of analysis used in offical control of the levels of dioxins (PCDD/PCDF) and dioxin-like PCBS in certain foodstuffs Repealed
  33. 1FIELD OF APPLICATION Repealed
  34. 2CLASSIFICATION OF METHODS BY THEIR DEGREE OF QUANTIFICATION Repealed
  35. 3BACKGROUND Repealed
  36. 4QUALITY ASSURANCE REQUIREMENTS Repealed
  37. 5REQUIREMENTS FOR LABORATORIES Repealed
  38. BASIC REQUIREMENTS TO BE MET BY ANALYTICAL PROCEDURE FOR DIOXINS (PCDD/FS) AND DIOXIN-LIKE PCBS Repealed
  39. 6.1Low working range and limits of quantification Repealed
  40. 6.2High selectivity (specificity) Repealed
  41. 6.3High accuracy (trueness and precision, bioassay apparent recovery) Repealed
  42. 6.4Validation in the range of level of interest and general quality control measures Repealed
  43. 6.5Limit of quantification Repealed
  44. 6.6Analytical criteria Repealed
  45. 6.7Specific requirements for screening methods Repealed
  46. SPECIFIC REQUIREMENTS FOR GC/HRMS METHODS TO BE COMPLIED WITH FOR SCREENING OR CONFIRMATORY PURPOSES Repealed
  47. 7.1General requirements Repealed
  48. 7.2Control of recoveries Repealed
  49. 7.3Removal of interfering substances Repealed
  50. 7.4Calibration with standard curve Repealed
  51. 8SPECIFIC REQUIREMENTS FOR BIOANALYTICAL METHODS Repealed
  52. Evaluation of the test response Repealed
  53. 8.1.1General requirements Repealed
  54. Calibration Repealed
  55. 8.1.2.1Calibration with standard curve Repealed
  56. 8.1.2.2Calibration with reference samples Repealed
  57. 8.1.3Separate determination of PCDD/Fs and dioxin-like PCBs Repealed
  58. 8.1.4Bioassay apparent recoveries Repealed
  59. 8.1.5Control of recoveries for clean-up Repealed
  60. 8.1.6Reporting limit Repealed
  61. 8.2Use of reference samples Repealed
  62. 8.3Determination of cut-off values Repealed
  63. 8.3.1Division 8.3.1 Repealed
  64. 8.3.2Division 8.3.2 Repealed
  65. 8.3.3Division 8.3.3 Repealed
  66. 8.3.4Restrictions to cut-off values: Repealed
  67. 8.4Performance characteristics Repealed
  68. REPORTING OF THE RESULT Repealed
  69. Confirmatory methods Repealed
  70. Bioanalytical screening methods Repealed
  71. to ANNEX IIIAppendix to ANNEX III Repealed
  72. Annex IV: Sample preparation and requirements for methods of analysis used in offical control of the levels of non-dioxin-like PCBs (PCB # 28, 52, 101, 138, 153, 180) in certain foodstuffs Repealed
  73. 1Applicable detection methods Repealed
  74. 2Identification and confirmation of analytes of interest Repealed
  75. 3Demonstration of performance of method Repealed
  76. 4Limit of quantification Repealed
  77. 5Quality control Repealed
  78. 6Control of recoveries Repealed
  79. 7Requirements for laboratories Repealed
  80. 8Performance characteristics: Criteria for the sum of the six indicator PCBs at the level of interest Repealed
  81. 9Reporting of results Repealed

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Signature

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IDEFINITIONSF1

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IIABBREVIATIONS USEDF1

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ISCOPEF1

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1PersonnelF1

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2Material to be sampledF1

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3Precautions to be takenF1

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4Incremental samplesF1

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5Preparation of the aggregate sampleF1

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6Replicate samplesF1

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7Packaging and transmission of samplesF1

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8Sealing and labelling of samplesF1

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IIISAMPLING PLANF1

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1Division of lots into sublotsF1

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2Number of incremental samplesF1

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3Specific provisions for the sampling of lots containing whole fishes of comparable size and weightF1

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4Sampling of lots of fish containing whole fishes of different size and/or weightF1

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5Sampling at retail stageF1

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1As regards non-dioxin-like PCBsF1

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2As regards dioxins (PCDD/PCDF) and dioxin-like PCBsF1

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VEXCEEDANCE OF ACTION LEVELSF1

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1FIELD OF APPLICATIONF1

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2CLASSIFICATION OF METHODS BY THEIR DEGREE OF QUANTIFICATIONF1

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3BACKGROUNDF1

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4QUALITY ASSURANCE REQUIREMENTSF1

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5REQUIREMENTS FOR LABORATORIESF1

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6.1Low working range and limits of quantificationF1

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6.2High selectivity (specificity)F1

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6.3High accuracy (trueness and precision, bioassay apparent recovery)F1

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6.4Validation in the range of level of interest and general quality control measuresF1

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6.5Limit of quantificationF1

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6.6Analytical criteriaF1

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6.7Specific requirements for screening methodsF1

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7.1General requirementsF1

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7.2Control of recoveriesF1

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7.3Removal of interfering substancesF1

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7.4Calibration with standard curveF1

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8SPECIFIC REQUIREMENTS FOR BIOANALYTICAL METHODSF1

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8.1.1General requirementsF1

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8.1.2.1Calibration with standard curveF1

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8.1.2.2Calibration with reference samplesF1

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8.1.3Separate determination of PCDD/Fs and dioxin-like PCBsF1

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8.1.4Bioassay apparent recoveriesF1

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8.1.5Control of recoveries for clean-upF1

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8.1.6Reporting limitF1

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8.2Use of reference samplesF1

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8.3Determination of cut-off valuesF1

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8.3.1F1

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8.3.2F1

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8.3.3F1

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8.3.4Restrictions to cut-off values:F1

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8.4Performance characteristicsF1

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Confirmatory methods

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Bioanalytical screening methods

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to ANNEX IIIF1

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1Applicable detection methodsF1

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2Identification and confirmation of analytes of interestF1

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3Demonstration of performance of methodF1

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4Limit of quantificationF1

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5Quality controlF1

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6Control of recoveriesF1

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7Requirements for laboratoriesF1

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8Performance characteristics: Criteria for the sum of the six indicator PCBs at the level of interestF1

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9Reporting of resultsF1

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