In order to implement the relevant work arrangements of the “Opinions of the General Office of the State Council on Comprehensively Deepening Pharmaceutical and Medical Device Supervision and Reform to Promote the High-Quality Development of the Pharmaceutical Industry”, support the export trade of medical device products, and standardize the handling of service matters for medical device export sales certificates issued by drug supervision and administration departments, the State Drug Administration organized and drafted the “Regulations on the Administration of Medical Device Export Sales Certificates”, and are now publicly soliciting comments from the public. The public comment period is from July 3 to August 2, 2025.

In order to implement the relevant work arrangements of the “Opinions of the General Office of the State Council on Comprehensively Deepening Pharmaceutical and Medical Device Supervision and Reform to Promote the High-Quality Development of the Pharmaceutical Industry”, support the export trade of medical device products, and standardize the handling of service matters for medical device export sales certificates issued by drug supervision and administration departments, the State Drug Administration organized and drafted the “Regulations on the Administration of Medical Device Export Sales Certificates”, and are now publicly soliciting comments from the public. The public comment period is from July 3 to August 2, 2025.