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當(dāng)前位置: 首頁 » 食品資訊 » 外訊導(dǎo)讀 » 歐盟就添加劑貝萊斯芽孢桿菌DSM 15544的授權(quán)延期申請發(fā)布意見

歐盟就添加劑貝萊斯芽孢桿菌DSM 15544的授權(quán)延期申請發(fā)布意見

放大字體  縮小字體 時間:2020-11-18 11:41 來源:食品伙伴網(wǎng) 作者: 澤夕   
核心提示:2020年11月13日,歐盟食品安全局(EFSA)發(fā)布消息,應(yīng)歐盟委員會要求,動物飼料添加劑和產(chǎn)品(FEEDAP)研究小組就貝萊斯芽孢桿菌(Bacillus velezensis)DSM 15544作為斷奶仔豬飼料添加劑的授權(quán)延期申請發(fā)表科學(xué)意見。
   食品伙伴網(wǎng)訊  2020年11月13日,歐盟食品安全局EFSA)發(fā)布消息,應(yīng)歐盟委員會要求,動物飼料添加劑和產(chǎn)品(FEEDAP)研究小組就貝萊斯芽孢桿菌(Bacillus velezensis)DSM 15544作為斷奶仔豬飼料添加劑的授權(quán)延期申請發(fā)表科學(xué)意見。
 
  經(jīng)過評估,專家組得出結(jié)論,在授權(quán)使用條件下,貝萊斯芽孢桿菌DSM 15544作為添加劑對目標(biāo)物種、消費者和環(huán)境都是安全的。該添加劑不是皮膚和眼睛刺激物或皮膚致敏劑,但應(yīng)視為呼吸道致敏劑。本授權(quán)續(xù)簽的申請中未包含修改或補充可能影響添加劑功效的原始授權(quán)條件的提案。因此,無需在授權(quán)更新的情況下評估添加劑的功效。
 
  部分原文報道如下:
 
  Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the assessment of the application for renewal of authorisation of Calsporin? (Bacillus velezensisDSM 15544) as a zootechnical additive for weaned piglets. The product under assessment is based on viable spores of a strain originally identified as Bacillus subtilis. During the course of the current assessment, the active agent has been reclassified as Bacillus velezensisDSM 15544. B. velezensis is considered suitable for the qualified presumption of safety (QPS) approach to safety assessment. The identity of the active agent was established and the compliance with the other qualifications /confirm/ied. Therefore, B. velezensisDSM 15544 is presumed safe for the target species, consumers of products derived from animals fed the additive and the environment. Since no concerns are expected from the other components of the additive, Calsporin? is also considered safe for the target species, consumers of products derived from animals fed the additive and the environment. The additive is not a dermal/eye irritant or a skin sensitiser but should be considered a respiratory sensitiser. The present application for renewal of the authorisation did not include a proposal for amending or supplementing the conditions of the original authorisation that would have an impact on the efficacy of the additive. Therefore, there was no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.
 
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日期:2020-11-18
 
 
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