Recently, the Bureau requested by the provincial bureau and then finish the registration of medicinal materials. The range of varieties of medicinal materials and then up by the drug regulatory department of the province issued approval number excipient species, aimed at strengthening the registration of medicinal materials management, and uniform re-registration approval of the text format. I notify the Board within the jurisdiction of medicinal materials manufacturers do a good job re-registration of medicinal materials preparation, and species-specific to enterprise personnel, plant facilities, formulation and process implementation, production site management, quality management and other aspects production site inspection, the existing problems require companies to implement rectification, then the successful completion of the registration of pharmaceutical excipients.

Previous: Registration of medicinal raw materials as early as the file system should try
Next： To participate in drug counseling mountains and rivers of China Pharmaceutical