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欧盟就添加剂酿酒酵母MUCL 39885的授权延期申请发布意见

   2020-11-12 食品伙伴网泽夕251
核心提示:   2020年11月9日,欧盟食品安全局(EFSA)发布消息,应欧盟委员会要求,动物饲料添加剂和产品(FEEDAP)研究小组就酿酒酵母(
     2020年11月9日,欧盟食品安全局(EFSA)发布消息,应欧盟委员会要求,动物饲料添加剂和产品(FEEDAP)研究小组就酿酒酵母(Saccharomyces cerevisiae)MUCL 39885作为断奶仔猪饲料添加剂的授权延期申请发表科学意见。 
  申请人已提供证据证明目前市场上的此种添加剂符合现有授权条件。经过评估,专家组得出结论,在授权使用条件下,酿酒酵母MUCL 39885作为添加剂对断奶仔猪、消费者和环境都是安全的。该添加剂被认为是潜在的皮肤和眼睛刺激物以及皮肤和呼吸系统敏感剂。在授权续期的情况下,无需对添加剂的有效性进行评估。
 
  部分原文报道如下:
 
  Following a request from the European Commission, the EFSA 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 the authorisation of the product Biosprint® (Saccharomyces cerevisiae MUCL 39885) as a feed additive for weaned piglets. Biosprint® is composed of only viable cells of Saccharomyces cerevisiae MUCL 39885. S. cerevisiae is considered by EFSA to have qualified presumption of safety status. The applicant has provided data demonstrating that the additive currently in the market complies with the conditions of the authorisation. The FEEDAP Panel confirms that the use of Biosprint® under the current authorised conditions of use is safe for weaned piglets, the consumers and the environment. The additive is considered as a potential skin and eye irritant and a skin and respiratory sensitiser. There is no need to assess the efficacy of Biosprint® in the context of the renewal of the authorisation.
 
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日期:2020-11-12
 
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