The Municipal Food and drug administration strengthens the supervision of extraction and extraction in the production of traditional Chinese medicine from four aspects

With the large-scale and intensive development of traditional Chinese medicine production, the problems existing in the extraction or outsourcing of traditional Chinese medicine extracts are more prominent, which brings hidden dangers to the quality and safety of traditional Chinese medicine In order to strengthen the supervision and management of extraction and extract of traditional Chinese medicine, standardize the production behavior of traditional Chinese medicine, and ensure the quality, safety and effectiveness of traditional Chinese medicine, the Municipal Food and Drug Administration strengthened the supervision of extraction and extract in the production of traditional Chinese medicine from four aspects First, standardize the extraction behavior of traditional Chinese medicine Chinese patent medicine manufacturing enterprises must have the ability to extract traditional Chinese medicine corresponding to their production varieties and scales According to the provisions of the State Administration, the whole province will stop the examination and approval of the entrusted processing of traditional Chinese medicine If it has been approved, it can continue processing until the validity of the approval documents, and no longer handle the extension after the expiration Second, to carry out the production and use of traditional Chinese medicine extracts for record Only when the approved prescription and preparation method are the varieties of Chinese herbal extracts, can they be produced by the way of extract feeding The production and use of relevant extracts shall be put on record according to the requirements Third, urge enterprises to implement quality responsibility The notice on strengthening the supervision and management of extraction and extraction in the production of traditional Chinese Medicine issued by the State Administration of the people's Republic of China shall be promptly communicated to relevant enterprises, and the publicity and training shall be intensified to improve the legal awareness, responsibility awareness and quality awareness of the Chinese patent medicine production enterprises, and urge them to consciously implement the management requirements of the State Administration of the people's Republic of China Fourth, strengthen daily supervision To establish corresponding regulatory files, formulate regulatory plans, and carry out extended or daily supervision to improve the regulatory efficiency.