Bampidis Vasileios, Azimonti Giovanna, Bastos Maria de Lourdes, Christensen Henrik, Dusemund Birgit, Kouba Maryline, Kos Durjava Mojca, López-Alonso Marta, López Puente Secundino, Marcon Francesca, Mayo Baltasar, Pechová Alena, Petkova Mariana, Ramos Fernando, Sanz Yolanda, Villa Roberto Edoardo, Woutersen Ruud, Anguita Montserrat, Galobart Jaume, Holczknecht Orsolya, Manini Paola, Tarrés-Call Jordi, Pettenati Elisa, Pizzo Fabiola
EFSA J. 2019 Nov 28;17(11):e05915. doi: 10.2903/j.efsa.2019.5915. eCollection 2019 Nov.
Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the assessment of the application for renewal of authorisation of the product Biosprint ( MUCL 39885) as a feed additive for dairy cows and horses. is considered by EFSA to have qualified presumption of safety (QPS) status. The applicant has provided data demonstrating that the additive currently in the market complies with the conditions of authorisation. The Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) Panel confirms that the use of Biosprint under the current authorised conditions of use is safe for the target species, the consumers and the environment. The additive is considered as a potential skin and eye irritant and skin/respiratory sensitiser. There is no need to assess the efficacy of Biosprint in the context of the renewal of the authorisation.
应欧盟委员会的要求，欧洲食品安全局被要求就产品Biosprint（MUCL 39885）作为奶牛和马的饲料添加剂的授权续展申请评估提供科学意见。欧洲食品安全局认为其具有合格的安全推定（QPS）地位。申请人提供的数据表明，目前市场上的添加剂符合授权条件。动物饲料添加剂和产品或物质专家小组（FEEDAP小组）确认，在当前授权使用条件下使用Biosprint对目标物种、消费者和环境是安全的。该添加剂被认为是一种潜在的皮肤和眼睛刺激物以及皮肤/呼吸道致敏剂。在授权续展的背景下，无需评估Biosprint的功效。
