Medical network - on January 3, on November 15, 2016, the state food and drug supervision and administration of taxation issued by the health food registration review work of examination and approval rules (2016 version) "(hereinafter referred to as detailed rules), has been clear about the review of health food registration approval procedures and requirements. In order to ensure the smooth and orderly the health food registration for examination and approval of the review work, now is to accept the application for registration before the implementation of the detailed rules for the review of the examination and approval matters notice is as follows:
A, "" health food raw materials directory (a)" and "allow health food says the health care function of directory (a)" (hereinafter referred to as the "directory") after the release, is to accept the filing management products, will be converted to the record management.
Second, is to accept the registration management scope of the new product registration and continue registration (registration) again to apply for, will be in accordance with the procedures prescribed by the detailed rules and the technology of product technical requirement organization review, and according to the review opinions to dole out additional information notice to the applicant. On July 1, 2018, the applicant can supplement data time according to the regulations of the original methods of 5 months time. Administration of state food and drug supervision and administration of health care food review center after receiving the applicant additional information, namely according to the "health food registration and filing management method" regulation time limit to complete the review of the work of examination and approval.
Three, is accepted by the registered scope changes (including the applicant's own name address change), technology transfer and reissue the certificate application, because of does not involve extend the time limit of the original registration approval, temporarily according to the original change, technology transfer, replacement procedures and requirements for examination and approval of the review, and approval documents issued the original format.
Please take note.
The food and drug supervision bureau |
