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Commission Directive 2002/69/EC (repealed)Show full title

Commission Directive 2002/69/EC of 30 July 2002 laying down the sampling methods and the methods of analysis for the official control of dioxins and the determination of dioxin-like PCBs in foodstuffs (Text with EEA relevance) (repealed)

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  1. Introductory Text

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    1. ANNEX I

      METHODS OF SAMPLING FOR OFFICIAL CONTROL OF THE LEVELS OF DIOXINS (PCDD/PCDF) AND THE DETERMINATION OF DIOXIN-LIKE PCBs IN CERTAIN FOODSTUFFS

      1. 1. Purpose and scope

      2. 2. Definitions

      3. 3. General provisions

        1. 3.1. Personnel

        2. 3.2. Material to be sampled

        3. 3.3. Precautions to be taken

        4. 3.4. Incremental samples

        5. 3.5. Preparation of the aggregate sample

        6. 3.6. Subdivision of aggregate sample in laboratory samples for enforcement, defence...

        7. 3.7. Packaging and transmission of aggregate and laboratory samples

        8. 3.8. Sealing and labelling of aggregate and laboratory samples

      4. 4. Sampling plans

        1. Number of incremental samples

        2. 4.1. Specific provisions for the sampling of lots containing whole fishes...

      5. 5. Compliance of the lot or sublot with the specification

    2. ANNEX II

      SAMPLE PREPARATION AND REQUIREMENTS FOR METHODS OF ANALYSIS USED IN OFFICIAL CONTROL OF THE LEVELS OF DIOXINS (PCDD/PCDF) AND THE DETERMINATION OF DIOXIN-LIKE PCBs IN CERTAIN FOODSTUFFS

      1. 1. Objective and field of application

      2. 2. Background

      3. 3. Quality assurance requirements to be complied with for sample preparation...

      4. 4. Requirements for laboratories

      5. 5. Requirements to be met by analytical procedure for dioxins and...

      6. 6. Specific requirements for GC/MS methods to be complied with for...

      7. 7. Screening methods of analysis

        1. 7.1. Introduction

          1. Screening approach

          2. Quantitative approach

        2. 7.2. Requirements for methods of analysis used for screening

        3. 7.3. Specific requirements for cell-based bioassays

        4. 7.4. Specific requirements for kit-based bioassays

      8. 8. Reporting of the result

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