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dc.contributor.authorRicci, Antonia
dc.contributor.authorAllende, Ana
dc.contributor.authorBolton, Declan
dc.contributor.authorChemaly, Marianne
dc.contributor.authorDavies, Robert
dc.contributor.authorHerman, Lieve
dc.contributor.authorKoutsoumanis, Kostas
dc.contributor.authorLindqvist, Roland
dc.contributor.authorNørrung, Birgit
dc.contributor.authorRobertson, Lucy
dc.contributor.authorRu, Giuseppe
dc.contributor.authorSanaa, Moez
dc.contributor.authorSimmons, Marion M
dc.contributor.authorSkandamis, Panagiotis
dc.contributor.authorSnary, Emma
dc.contributor.authorSpeybroeck, Niko
dc.contributor.authorTer Kuile, Benno
dc.contributor.authorThrelfall, john
dc.contributor.authorWahlström, Helene
dc.contributor.authorGirones, Rosina
dc.contributor.authorAlvarez Ordoñez, Avelino
dc.contributor.authorGriffin, John
dc.contributor.authorCorreia, Sandra
dc.contributor.authorFernandez Escamez, Pablo Salvador
dc.date.accessioned2019-01-03T14:45:47Z
dc.date.available2019-01-03T14:45:47Z
dc.date.created2018-12-26T12:44:46Z
dc.date.issued2018
dc.identifier.issn1831-4732
dc.identifier.urihttp://hdl.handle.net/11250/2579062
dc.description.abstractEFSA received an application from the Dutch Competent Authority, under Article 20 of Regulation (EC)No 1069/2009 and Regulation (EU) No 142/2011, for the evaluation of an alternative method fortreatment of Category 3 animal by-products (ABP). It consists of the hydrolysis of the material to short-carbon chains, resulting in medium-chain fatty acids that may contain up to 1% hydrolysed protein, foruse in animal feed. A physical process, with ultrafiltration followed by nanofiltration to remove hazards, isalso used. Process efficacy has been evaluated based on the ability of the membrane barriers to retainpotential biological hazards present. Small viruses passing the ultrafiltration membrane will be retained atthe nanofiltration step, which represents a Critical Control Point (CCP) in the process. This step requiresthe Applicant to validate and provide certification for the specific use of the nanofiltration membranesused. Continuous monitoring and membrane integrity tests should be included as control measures in theHACCP plan. The ultrafiltration and nanofiltration techniques are able to remove particles of the size ofvirus, bacteria and parasites from liquids. If used under controlled and appropriate conditions, theprocessing methods proposed should reduce the risk in the end product to a degree which is at leastequivalent to that achieved with the processing standards laid down in the Regulation for Category 3material. The possible presence of small bacterial toxins produced during the fermentation steps cannotbe avoided by the nanofiltration step and this hazard should be controlled by a CCP elsewhere in theprocess. The limitations specified in the current legislation and any future modifications in relation to theend use of the product also apply to this alternative process, and no hydrolysed protein of ruminantorigin (except ruminant hides and skins) can be included in feed for farmed animals or for aquaculture.nb_NO
dc.language.isoengnb_NO
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleEvaluation of the application for a new alternative processing method for animal by‐products of Category 3 material (ChainCraft B.V.)nb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.volume16nb_NO
dc.source.journalEFSA Journalnb_NO
dc.source.issue6nb_NO
dc.identifier.doi10.2903/j.efsa.2018.5281
dc.identifier.cristin1647156
cristin.unitcode192,16,2,0
cristin.unitnameInstitutt for mattrygghet og infeksjonsbiologi
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
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