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In order to thoroughly implement the major decisions and deployments of the Party Central Committee and the State Council on deepening the reform of "license separation", optimize the business environment, further stimulate the vitality of the development of market entities, improve the application service level of the State Food and Drug Administration's "Internet + drug supervision", and provide enterprises with more efficient and convenient government services
.
After research, it has been decided that from November 1, 2022, the electronic certificate for batch issuance of biological products and the electronic approval documents for experimental research of narcotic drugs and psychotropic substances will be officially used, and the relevant matters are hereby announced as follows: 1.
From November 1, 2022, electronic licenses will be used for the batch issuance certificates of biological products and the approval documents for experimental research of narcotic drugs and psychotropic substances
.
After the implementation of electronic licenses, they will be delivered when the push is successful, and paper licenses will no longer be issued in principle
.
2.
Electronic certificates for the batch issuance of biological products, electronic approvals for experimental research projects on narcotic drugs and psychotropic substances have the same legal effect
as paper licenses.
Electronic certificates and electronic approvals have functions
such as instant delivery, SMS reminder, license authorization, scan code query, online verification, and network-wide sharing.
3.
The applicant must first register in the online office hall of the State Food and Drug Administration and verify his real name, and properly keep the relevant account number, electronic certificate and electronic approval documents
.
4
.
Applicants can enter the "My License" column of the legal person space in the online office hall, or log in to the "China Food and Drug Administration APP" to view and download the corresponding electronic certificates and electronic approvals.
For answers to frequently asked questions about electronic licenses, please refer to the "Electronic License FAQs" column in the online office hall of the State Food and Drug Administration
.
This is hereby announced
.
NMPA September 30, 2022
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