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The comprehensive Department of the State Food and Drug Administration publicly solicited opinions on the classification rules of in vitro diagnostic reagents (Draft for comments)
2021-9-4


In order to prepare and revise the supporting regulations of the regulations on the supervision and administration of medical devices, the State Food and drug administration has organized the drafting of the classification rules for in vitro diagnostic reagents (Draft for comments) (see the annex), and is now seeking comments from the public.

Please feedback your comments to email: mdct@nmpa.gov.cn 。 Please indicate "feedback on reagent classification rules" at the subject of the email.

The deadline for feedback is May 31, 2021.




Annex:classification rules for in vitro diagnostic reagents (Draft for comments)