MRL setting and intakes for cereals. Annette Petersen

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Transcription:

MRL setting and intakes for cereals Annette Petersen

2 Who am I Senior adviser at the National Food Institute Many years experience from the laboratory MRL setting and risk assessment (no laboratory work anymore) Responsible for the homepage for cereals and feeds

3 Legislation All MRLs are now harmonised: only set or amend MRLs at the EU level Regulation 396/2005 MRLs in regulation 149/2008 and 839/2009 Commodities in regulation 178/2006 Regulation 396/2005 covers both food and feed tomorrow about feed

4 What is needed to set a MRL Residue definition in relevant plants: Which substances are included in the MRLs Which substances shall be determined in the monitoring E.g. residue definition for parathion-methyl is: Sum of parathion-methyl and paraoxon-methyl expressed as parathion-methyl Independent validated method for all substances included in the residue definition Two different laboratories have validated the method

5 What is needed to set a MRL MRLs in cereals are set on the background of residue trials conducted according to critical Good Agricultural Practice (GAP): Max. application rate Max. number of treatments Shortest time between treatments Shortest time between treatment and harvest IMPORTANT: Setting MRLs in raw agricultural commodity (RAC) e.g. MRL in grain not in flour or bread Calculate back to RAC from flour and bread

6 What is needed to set a MRL At least 8 residue trials for major crops and 4 for minor and very minor crops Europe divided in North and South zone (under discussion) Major crops in whole Europe Barley, maize, oat, rye, triticale, wheat Major in South: Rice and sorghum All other cereals are minor or very minor

7 What is needed to set a MRL Enough residue trials from both Northern and Southern countries if uses both places E,g, 8 trials from each if a major crop The trials have to be performed Different years Different places/countries

8 Extrapolation Can extrapolate results from residue trials from one commodity to another Not necessary to perform trials for all commodities Only extrapolate if GAPs are similar Same number of treatments, same application rate ± 25 %; E.g. 100 g/ha 75-125 g/ha Dependent on time of treatment Before or after flowering Seed treatment Post-harvest

9 Extrapolation Used close to harvest, after consumable parts are developed (before or after blossom) Barley oat Wheat rye and triticale Maize sorghum and millet Used early in growing season Barley, oats, rye, triticale, wheat each other Maize sorghum, millet

10 MRL setting for plants Two ways of performing calculations for MRL setting Rmax = R + k x s It is assumed that the residues follow a normal distribution R = mean of residues s = standard deviation of residues k = factor Rcal: a non-parametric method (not shown) Rank the residues

11 MRL setting for plants 8 residue trials: 0.2, 0.21, 0.29, 0.36, 0.46, 0.55, 0.66, 1.13 mg/kg Rcal = 1.27 Rmax = 0.483 + (3.188 x 0.0.308) = 1.46 R = 0.483 s = 0.308 k (n = 8) = 3.188 Proposal: 2 mg/kg Calculate for both for North and South

12 Risk assessment: Chronic exposure Risk assessment performed by comparing the chronic intake with the Acceptable Daily Intake for the pesticide Chronic: Whole life Use average for consumption and content The intake is calculated including all MRLs Intake < ADI: no problems Intake > ADI: Refinements If intake > ADI after refinements: Discussions on what to do What uses should be deleted?

13 Risk assessment: Chronic exposure Refinements: Use median from residue trials in stead of MRL Processing for example: Brewing Baking Peeling (e.g. citrus fruits, pineapple, and banana)

14 Risk assessment: Acute exposure Acute or short term Intake is compared with Acute Reference Dose Calculated for each commodity at a time Use high intake and MRL Different formulas are used depending on commodity Acute intake < ARfD: no problems Acute intake > ARfD: Refinements Acute intake > ARfD after refinements: No approval Refinement: Processing Highest residue in stead of MRL

15 Intake European Food Safety Authorisation (EFSA) has collected consumption data from EU Member States Database available on the internet Put the residue data into the database and both the chronic and acute intake are calculated

16 EU monitoring programme EU monitoring programme also includes cereals EFSA has now the responsibility of the monitoring programme Meeting in October about the programme Expect that there will come some changes (reporting the results, what is the results used for)

Thank you for your attention 17