What does compulsory examination of patented drugs and medical devices mean?

Inspection by relevant departments.

The relevant departments shall formulate national standards for the technical requirements that need to be unified throughout the country in regular inspection. For technical requirements that need to be unified within a certain industry in the country without national standards, industry standards can be formulated. The standards for the protection of human health and property and the standards for enforcement stipulated by laws and administrative regulations are mandatory standards, while other standards are recommended standards. Mandatory standards must be implemented.