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The General Department of the State Food and Drug Administration publicly solicits opinions on the "Check Points for Drug Marketing Authorization Holders (Draft for Comment)"

 Last Update: 2022-04-27
 Source: Internet
 Author: User

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In order to implement the Drug Administration Law of the People's Republic of China and the Vaccine Administration Law of the People's Republic of China, and fully implement the safety, effectiveness and quality assurance of the drug marketing authorization holder in the whole process of drug development, production, distribution and use, To further standardize the supervision and inspection of drug marketing authorization holders, the State Food and Drug Administration organized the drafting of the "Check Points for Drug Marketing Authorization Holders (Draft for Comment)", which is now open to the public for comments
.

Please submit relevant comments via email to ypjgs@nmpa.

Attachment: Check Points for Drug Marketing Authorization Holders (Draft for Comment)

General Department of the State Food and Drug Administration

March 28, 2022

Attachment.

Attachment.
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