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當(dāng)前位置: 首頁 » 食品資訊 » 外訊導(dǎo)讀 » 歐盟評(píng)估乳酸腸球菌NCIMB 11181作為斷奶仔豬等物種飼料添加劑的授權(quán)更新...

歐盟評(píng)估乳酸腸球菌NCIMB 11181作為斷奶仔豬等物種飼料添加劑的授權(quán)更新申請(qǐng)

放大字體  縮小字體 時(shí)間:2023-12-04 15:38 來源:食品伙伴網(wǎng) 作者: 澤夕   
核心提示:2023年12月1日,歐盟食品安全局(EFSA)發(fā)布消息,歐盟食品安全局(EFSA)發(fā)布關(guān)于乳酸腸球菌(Enterococcus lactis)NCIMB 11181作為飼養(yǎng)用于斷奶仔豬、育肥犢牛和飼養(yǎng)犢牛飼料添加劑的授權(quán)更新申請(qǐng)的評(píng)估。
   食品伙伴網(wǎng)訊  2023年12月1日,歐盟食品安全局EFSA)發(fā)布消息,歐盟食品安全局(EFSA)發(fā)布關(guān)于乳酸腸球菌(Enterococcus lactis)NCIMB 11181作為飼養(yǎng)用于斷奶仔豬、育肥犢牛和飼養(yǎng)犢牛飼料添加劑的授權(quán)更新申請(qǐng)的評(píng)估。
 
  經(jīng)過評(píng)估,專家小組得出結(jié)論,該添加劑在授權(quán)使用條件下對(duì)目標(biāo)物種、消費(fèi)者和環(huán)境都是安全的。在授權(quán)更新的情況下,無需評(píng)估添加劑的功效。部分原文報(bào)道如下:
 
  Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the assessment of the application for renewal of the authorisation of Enterococcus lactis NCIMB 11181 (Lactiferm®) as a zootechnical additive for weaned piglets, calves for fattening and calves for rearing. The product under assessment is based on a strain originally identified as Enterococcus faecium. During the current assessment, the active agent has been reclassified as Enterococcus lactis. The additive currently authorised is marketed in two formulations: Lactiferm Basic 50 (a solid formulation to be used in feed), and Lactiferm WS200 (a solid ‘water-soluble’ formulation to be used in water for drinking). The applicant has provided evidence that the additive currently on the market complies with the existing conditions of authorisation. The Panel concludes that the use of Lactiferm® under the authorised conditions of use remains safe for the target species (calves up to 6 months and weaned piglets up to 35 kg), consumers and the environment. The Lactiferm WS200 formulation of the additive is not irritant to skin or eyes. Owing to the proteinaceous nature of the active agent, both formulations of the additive are considered respiratory sensitisers. It is not possible to conclude on the irritating potential for skin and eyes of the Lactiferm Basic 50 formulation or on the potential of both forms of the additive to cause skin sensitisation. There is no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.
 
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日期:2023-12-04
 
 
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