It means that pharmaceutical production units must meet a series of standards set by the state in terms of software (personnel) and hardware (facilities, equipment, and premises), and follow the norms set by the state in their daily production operations.
China's drug production is subject to mandatory GMP certification, which means that pharmaceutical companies must be GMP-certified before they can produce drugs.
GMP certification is ready to produce drugs before the manufacturer to the "State Food and Drug Administration (SFDA)" to submit an application for certification materials, the SFDA will be in the specified working days to send a GMP inspection team to the factory site visits, and then based on the results of the inspection against the GMP requirements to determine whether the manufacturer meets the GMP standards. Determine whether the manufacturer meets the standards of GMP, in line with the manufacturers through the GMP certification, you can carry out production activities; does not meet the need for rectification (small problems) or rectification (big problems)
This is quite a complex, not a sentence or two can be explained
National healthcare mandatory certification and:
GSP "Good Manufacturing Practice"
GAP "Good Manufacturing Practice"
GMP "Good Manufacturing Practice"
GAP "Good Manufacturing Practice"
GAP "Chinese herbal medicine production quality management norms"
GCP "drug clinical trial quality management norms"
GLP "drug non-clinical research quality management norms"
GUP<< drug use quality management norms>>
Specifically, you can refer to the following link information