The National Medical Products Administration publicly solicits opinions on the "Guidelines for Inspection of Medical Device Production Quality Management Standards (Draft for Comments)"

To implement the "Regulations on the Supervision and Administration of Medical Devices," the "Measures for the Supervision and Administration of Medical Device Production," and the "Good Manufacturing Practice for Medical Devices," and to standardize and guide the inspection of medical device production, the National Medical Products Administration has organized the drafting of the "Guiding Principles for Inspection of Medical Device Production Quality Management Standards (Draft for Comments)." The draft is now open to the public for comments. The public comment period is from June 9, 2026, to June 24, 2026.
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