ANNEX IIIU.K. SAMPLING AND ANALYSIS REQUIREMENTS FOR THE MONITORING REFERRED TO IN ARTICLE 4

I. Sampling U.K.

1.The sample shall be representative for the sampled batch.U.K.

2.FBOs shall ensure that they undertake representative sampling and analysis of their products for the presence of acrylamide to verify the effectiveness of mitigation measures, i.e. the levels of acrylamide are consistently below the benchmark levels.U.K.

3.FBOs shall ensure that a representative sample of each product type is taken for analysis of acrylamide concentration. A ‘product type’ includes groups of products with the same or similar ingredients, recipe design, process design and/or process controls where these have a potential influence acrylamide levels in the finished product. Monitoring programmes shall prioritise product types that have the demonstrated potential to exceed the benchmark level and shall be risk-based where further mitigation measures are feasible.U.K.

II. Analysis U.K.

1.FBOs shall provide sufficient data to enable an assessment of the level of acrylamide and of the likelihood that the product type might exceed the benchmark level.U.K.

2.The sample shall be analysed in a laboratory that participates in appropriate proficiency testing schemes (which comply with the ‘International Harmonised Protocol for the Proficiency Testing of (Chemical) Analytical Laboratories’(1) developed under the auspices of IUPAC/ISO/AOAC) and uses approved analytical methods for detection and quantification. Laboratories shall be able to demonstrate that they have internal quality control procedures in place. Examples of these are the ‘ISO/AOAC/IUPAC Guidelines on Internal Quality Control in Analytical Chemistry Laboratories’(2).U.K.

Wherever possible the trueness of analysis shall be estimated by including suitable certified reference materials in the analysis.

3.The method of analysis used for the analysis of acrylamide must comply with the following performance criteriaU.K.

ParameterCriterion
ApplicabilityFoods specified in this Regulation
SpecificityFree from matrix or spectral interferences
Field blanksLess than Limit of Detection (LOD)
Repeatability (RSDr)0,66 times RSDR as derived from (modified) Horwitz equation
Reproducibility (RSDR)as derived from (modified) Horwitz equation
Recovery75-110 %
Limit of Detection (LOD)Three tenths of LOQ
Limit of Quantification (LOQ)

For benchmark level < 125 μg/kg: ≤ two fifths of the benchmark level (however not required to be lower than 20 μg/kg)

For benchmark level ≥ 125 μg/kg: ≤ 50 μg/kg

4.Analysis of acrylamide can be replaced by measurement of product attributes (e.g. colour) or process parameters provided that a statistical correlation can be demonstrated between the product attributes or process parameters and the acrylamide level.U.K.

III. Frequency of sampling U.K.

1.FBOs shall, undertake sampling and analysis at least annually for products that have a known and well-controlled acrylamide level. FBOs shall carry out higher frequency sampling and analysis of products having the potential to exceed the benchmark level and shall be risk-based where further mitigation measures are feasible.U.K.

2.Based on this assessment referred to in point II.1, the FBOs shall specify appropriate frequencies for analysis for each product type. The assessment shall be repeated if a product or process is modified in a way that could lead to a change in the acrylamide level in the final product.U.K.