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Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances present in food of animal origin

EFSA was asked by the European Commission to update the Scientific Opinion on methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances in food of animal origin. This guidance doc...

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Autores principales: Knutsen, Helle Katrine, Alexander, Jan, Barregård, Lars, Bignami, Margherita, Brüschweiler, Beat, Ceccatelli, Sandra, Cottrill, Bruce, Dinovi, Michael, Edler, Lutz, Grasl‐Kraupp, Bettina, Hogstrand, Christer, Nebbia, Carlo Stefano, Oswald, Isabelle P, Petersen, Annette, Rose, Martin, Roudot, Alain‐Claude, Schwerdtle, Tanja, Vollmer, Günter, Vleminckx, Christiane, Wallace, Heather, Filipič, Metka, Fürst, Peter, O'Keeffe, Michael, Penninks, André, Van Leeuwen, Rolaf, Baert, Katleen, Hoogenboom, Laurentius (Ron)
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7009670/
https://www.ncbi.nlm.nih.gov/pubmed/32625970
http://dx.doi.org/10.2903/j.efsa.2018.5332
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author Knutsen, Helle Katrine
Alexander, Jan
Barregård, Lars
Bignami, Margherita
Brüschweiler, Beat
Ceccatelli, Sandra
Cottrill, Bruce
Dinovi, Michael
Edler, Lutz
Grasl‐Kraupp, Bettina
Hogstrand, Christer
Nebbia, Carlo Stefano
Oswald, Isabelle P
Petersen, Annette
Rose, Martin
Roudot, Alain‐Claude
Schwerdtle, Tanja
Vollmer, Günter
Vleminckx, Christiane
Wallace, Heather
Filipič, Metka
Fürst, Peter
O'Keeffe, Michael
Penninks, André
Van Leeuwen, Rolaf
Baert, Katleen
Hoogenboom, Laurentius (Ron)
author_facet Knutsen, Helle Katrine
Alexander, Jan
Barregård, Lars
Bignami, Margherita
Brüschweiler, Beat
Ceccatelli, Sandra
Cottrill, Bruce
Dinovi, Michael
Edler, Lutz
Grasl‐Kraupp, Bettina
Hogstrand, Christer
Nebbia, Carlo Stefano
Oswald, Isabelle P
Petersen, Annette
Rose, Martin
Roudot, Alain‐Claude
Schwerdtle, Tanja
Vollmer, Günter
Vleminckx, Christiane
Wallace, Heather
Filipič, Metka
Fürst, Peter
O'Keeffe, Michael
Penninks, André
Van Leeuwen, Rolaf
Baert, Katleen
Hoogenboom, Laurentius (Ron)
collection PubMed
description EFSA was asked by the European Commission to update the Scientific Opinion on methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances in food of animal origin. This guidance document presents a simple and pragmatic approach which takes into account both analytical and toxicological considerations. The RPA shall be based on the reasonably achievable lowest residue concentration that can unequivocally be determined by official control laboratories, i.e. the reasonably achievable lowest decision limit (CCα). The aim is to check whether this concentration is low enough to adequately protect the consumers of food commodities that contain that substance. The proposed step‐wise approach applies toxicological screening values (TSVs), based on genotoxic potential, pharmacological activity, as well as other effects of the substance. The highest dietary exposure corresponding to the reasonably achievable lowest CCα for the substance has to be estimated and compared with the TSV. Where equal to or lower than the TSV, the reasonably achievable lowest CCα can be accepted as the RPA. If higher, the sensitivity of the analytical method needs to be improved. In the case where no further analytical improvements are feasible within a short to medium time frame, a substance‐specific risk assessment should be considered. This also applies when the potential adverse effects do not allow use of the decision tree, as for high potency carcinogens, inorganic substances or compounds with allergenic effects or causing blood dyscrasias. The CONTAM Panel concluded that RPAs should be food matrix independent. RPAs cannot be applied to non‐edible matrices, which are also monitored for non‐allowed pharmacologically active substances.
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spelling pubmed-70096702020-07-02 Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances present in food of animal origin Knutsen, Helle Katrine Alexander, Jan Barregård, Lars Bignami, Margherita Brüschweiler, Beat Ceccatelli, Sandra Cottrill, Bruce Dinovi, Michael Edler, Lutz Grasl‐Kraupp, Bettina Hogstrand, Christer Nebbia, Carlo Stefano Oswald, Isabelle P Petersen, Annette Rose, Martin Roudot, Alain‐Claude Schwerdtle, Tanja Vollmer, Günter Vleminckx, Christiane Wallace, Heather Filipič, Metka Fürst, Peter O'Keeffe, Michael Penninks, André Van Leeuwen, Rolaf Baert, Katleen Hoogenboom, Laurentius (Ron) EFSA J Guidance EFSA was asked by the European Commission to update the Scientific Opinion on methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances in food of animal origin. This guidance document presents a simple and pragmatic approach which takes into account both analytical and toxicological considerations. The RPA shall be based on the reasonably achievable lowest residue concentration that can unequivocally be determined by official control laboratories, i.e. the reasonably achievable lowest decision limit (CCα). The aim is to check whether this concentration is low enough to adequately protect the consumers of food commodities that contain that substance. The proposed step‐wise approach applies toxicological screening values (TSVs), based on genotoxic potential, pharmacological activity, as well as other effects of the substance. The highest dietary exposure corresponding to the reasonably achievable lowest CCα for the substance has to be estimated and compared with the TSV. Where equal to or lower than the TSV, the reasonably achievable lowest CCα can be accepted as the RPA. If higher, the sensitivity of the analytical method needs to be improved. In the case where no further analytical improvements are feasible within a short to medium time frame, a substance‐specific risk assessment should be considered. This also applies when the potential adverse effects do not allow use of the decision tree, as for high potency carcinogens, inorganic substances or compounds with allergenic effects or causing blood dyscrasias. The CONTAM Panel concluded that RPAs should be food matrix independent. RPAs cannot be applied to non‐edible matrices, which are also monitored for non‐allowed pharmacologically active substances. John Wiley and Sons Inc. 2018-07-24 /pmc/articles/PMC7009670/ /pubmed/32625970 http://dx.doi.org/10.2903/j.efsa.2018.5332 Text en © 2018 European Food Safety Authority. EFSA Journal published by John Wiley and Sons Ltd on behalf of European Food Safety Authority. https://creativecommons.org/licenses/by-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nd/4.0/ (https://creativecommons.org/licenses/by-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited and no modifications or adaptations are made.
spellingShingle Guidance
Knutsen, Helle Katrine
Alexander, Jan
Barregård, Lars
Bignami, Margherita
Brüschweiler, Beat
Ceccatelli, Sandra
Cottrill, Bruce
Dinovi, Michael
Edler, Lutz
Grasl‐Kraupp, Bettina
Hogstrand, Christer
Nebbia, Carlo Stefano
Oswald, Isabelle P
Petersen, Annette
Rose, Martin
Roudot, Alain‐Claude
Schwerdtle, Tanja
Vollmer, Günter
Vleminckx, Christiane
Wallace, Heather
Filipič, Metka
Fürst, Peter
O'Keeffe, Michael
Penninks, André
Van Leeuwen, Rolaf
Baert, Katleen
Hoogenboom, Laurentius (Ron)
Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances present in food of animal origin
title Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances present in food of animal origin
title_full Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances present in food of animal origin
title_fullStr Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances present in food of animal origin
title_full_unstemmed Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances present in food of animal origin
title_short Update: methodological principles and scientific methods to be taken into account when establishing Reference Points for Action (RPAs) for non‐allowed pharmacologically active substances present in food of animal origin
title_sort update: methodological principles and scientific methods to be taken into account when establishing reference points for action (rpas) for non‐allowed pharmacologically active substances present in food of animal origin
topic Guidance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7009670/
https://www.ncbi.nlm.nih.gov/pubmed/32625970
http://dx.doi.org/10.2903/j.efsa.2018.5332
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