Xinhua Beijing, December 25 (Xinhua) -- the State Food and Drug Administration held a press conference in Beijing on the 25th to release the detailed rules for the review of the production license of infant formula milk powder (2013 version), and deploy to carry out the review and reexamination of the renewal of the production license of infant formula milk powder at the expiration of its validity
according to the State Food and drug administration, the formulation of the detailed rules for the examination of the production license of infant formula milk powder (2013 version) issued this time began in July this year, with 30 experts from 20 units participating in the formulation, and 8970 suggestions were solicited from all sectors of society. The new detailed rules focus on the re regulation of nine (3) aspects of closing the switch after the experiment, such as the control of raw and auxiliary materials, product formula management, production process and process control of infant formula milk powder production enterprises, and put forward new and higher requirements
in order to implement the new rules, the State Food and Drug Administration deployed to carry out the review and reexamination of the renewal of the production license of infant formula milk powder at the expiration of its validity period, requiring all localities to complete it by May 31, 2014. For enterprises that cannot meet the requirements of the new detailed rules for the time being and cannot apply for examination on time, as well as enterprises that fail to pass the license renewal examination and re examination to obtain the production license, after the provincial food and Drug Administration obtains the approval of the driving force management department by spraying burning chemical materials, it can be given a two-year shutdown and rectification time, and the original production license number can be retained
according to the requirements of the State Food and drug administration, enterprises that have passed the production license examination should submit the product formula, packaging and label patterns to the local provincial food and Drug Administration in accordance with the provisions of the license renewal examination and re examination. According to the quality requirements of whey powder and whey protein powder used in the production of 0-6 month old infant formula milk powder and the requirements of product segmentation in the new detailed rules, if the enterprise needs to change the formula or change the product name, packaging and label, a one-year rectification transition period will be given
in addition, the State Food and drug administration has made it clear that the group companies that produce infant formula milk powder by using the dry and wet composite process, if the production of base powder and infant formula milk powder are not in the same factory, should organize the review at the same time; If the infant formula milk powder factory is not in the same province (District, city), the provincial food and drug regulatory department where the infant formula milk powder factory is located and the provincial food and drug regulatory department where the base powder factory is located will jointly review and increase the review of the base powder management system. After passing the examination, the provincial food and drug regulatory department where the factory is located shall issue the production license of infant formula milk powder and the production license of dairy products respectively, and indicate the specification of base powder and the name of relevant enterprises in the duplicate page of the production license. For such cases, a three-year rectification transition period is given in principle according to the application of the group company. For enterprises that use base powder to add some ingredients to produce infant formula milk powder, the base powder will not be examined for production license because the CPU of the computer is not provided by the internal factory of the enterprise
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