MED-(English version) What considerations should be taken when replacing the biological test report of the applied product with the biological test report of the predicate devices marketed by the company?

MED-(Bi)Opinions of CFDA on Promoting Food and Drug Producers and Traders to Improve Traceability System

MED-(Chinese Version) Notice by General Office of CFDA on the Issuance of 2017 Medical Device Industry Standard Revision Project

MED-(English Version) Circular of CFDA General Office[2016]No117_Relevant Problems Concerning Word Change of In Vitro Diagnosis Reagent Manual