Mushonga

michmiishonga nemidziyo inoita basa rakakosha mukugadzira, uye sekuburitsa, basa revharuvhu intenderera mukuvhara mhepo, kutakura zvinhu kwakakoshawo mumafekitori makuru emishonga。Kutanga kubva kuzvinhu, maitiro, chimiro uye EHS, kambani inogadzira uye inogadzira seti yakazara ye模块化旋转mavharuvhu ayo asina chepfu, asina mhedzisiro uyeo akazara zvinoenderana国家标准GB28670-2012通用《药品生产质量管理实施规范制药机械(设备)》，《药品生产质量管理规范》(GMP)是我国药品生产管理的重要内容。