The State Food and Drug Administration released the quality supervision status of infant formula mil

发布时间:1970-01-01

In December 2013, the General Administration issued the "Detailed Rules for the Examination of Production Licensing of Infant Formula Milk Powder (2013 Edition)". In accordance with the requirements of the detailed rules, the General Administration has deployed various regions to carry out the inspection and re-examination of the production license of infant formula milk powder, and carried out the inspection of the production license of 133 infant formula milk powder manufacturers across the country. As of May 29, a total of 82 enterprises across the country have obtained production licenses, produced 1,638 types of infant formula milk powder products, and 51 enterprises that have not passed the review, applied for extension or cancellation.

In order to improve the production and operation licensing, quality and safety assurance, and corporate responsibility of infant formula milk powder enterprises, the State Administration has formulated the "Infant formula milk powder production license review rules (2013 version)" and deployed for renewal review and renewal. Audit work. With reference to the drug management model, Good Manufacturing Practices (GMP) for powdered infant formula foods have been implemented, and the relevant review system for the use of infant formula milk powder product formulas and raw materials has been established and implemented. Strengthen the supervision and management of the sales of infant formula milk powder, strengthen the licensing management of business units in the circulation field, and promote the pilot sales of infant formula milk powder in pharmacies. These institutional measures will ensure that infant formula milk powder implements the entire process and the entire chain of supervision.