英文保健食品常见问题汇总

F the function research report should include the function name, applying reasons, functional testing methods and evaluation results. If the company cannot proceed animal or human test, it must illustrate the reasons and provide related documents on the functional report. Tianjianhuacheng: We recommend one product dont have more than two functions, and different functions need to have some sorts of connections, otherwise it is hard to pass. Besides, apply for the new function is VERY hard to provide documents accepted by CFDA, so the risk is very high. 11. Requirements of the name of the health food Tianjianhuacheng: Each product can only have one name, and the name should be consisted by trade name, generic name and attribute name, a series product must have the same trade name and generic name. Generally speaking, company should use the main raw material as the products name, and use scientific and standard name of raw material, but words numbers are no more than 10. The product cannot use the words like treatment, the exaggerate words like high efficiency, the words of human organs, peoples name and address, the special group and the letter, number, symbols and others. 12. The requirements of the manufacture company Tianjianhuacheng: During the health food CFDA registration, applicant does not need to have his own manufacture factory, and the applicant can use the authorization kind of manufacture. And after applicant receive the approval certificate, the applicant can have their own manufacture or authorize other companies to manufacture. In any kind of manufacture, the manufacture companies must have the “health food hygiene license” and confirm to “health food GMP” (on the valid date), besides, the manufacture should have the manufacture facilities according with the type of the health food. After CFDA accept the application, it will send staffs to production site to evaluate manufacture process and recorded documents, and check the reality, normative and integrity of the health food. As for the imported products, the foreign manufacture company must conform to local GMP requirements. And CFDA will arrange production site investigate work. 13. The requirements of the auxiliary material of the health food Tianjianhuacheng: The auxiliary material, usage amount should confirm to Chinese related laws. CFDA published or approved raw and auxiliary materials can be used in the health food. In addition, the above materials and the usage amount should confirm to Chinese related health food laws. Many products cannot achieve CFDA approval certificate, one of the most important reasons is that the raw materials dont confirm to Chinese laws: the materials of the health food must be allowed in China and confirm to hygiene standards, if not, the products may not pass the products tests and ingredients evaluation. Tianjianhuacheng: The product should be evaluated before testing, and does the basis work at the beginning, then the product will have a high possibility to get CFDA certificate. In conclusion, the laws of health food CFDA registration have been changed ALL the time, and CFDA still asks for opinions from the public of the related laws which may issued in 2014. So it is