According to the Regulations on the Administration of Drug Import and Export Licenses:
3, import and export units in the customs formalities, should submit a joint declaration form, and apply to the customs for cancellation of the joint declaration form. The customs shall examine the import license and export license, and affix the "Inspection Seal" on the customs declaration form and return it to the import and export unit.
After the import and export is completed 1 month, the import and export unit shall return the first copy of the import license or export license issued by the customs and the customs declaration form to the license issuing agency.
4. The validity of the Drug Import License is 1 year.
The validity period of the Drug Export License shall not exceed 3 months (the validity period shall not exceed one year).
5. The drug import license and export license shall be subject to the management of "one license and one customs clearance", which can only be used once within the validity period, and the contents of the license shall not be changed. If the import and export are postponed for some reason, the renewal formalities can be extended with the original import and export license.
6. Where protein assimilation preparations and peptide hormones are imported or exported by processing trade, the customs shall verify the import license and export license, and go through customs clearance procedures as required. If it is really impossible to export due to special circumstances, it shall be handled by the (food) drug supervision and administration department at the place where the goods are handed over in accordance with the regulations, and the customs shall review the relevant certification materials and go through the verification procedures in accordance with the regulations.
Extended data:
According to the Drug Administration Law of People's Republic of China (PRC):
Article 17 When purchasing drugs, pharmaceutical trading enterprises must establish and implement the system of inspection and acceptance of incoming goods, and verify the marks such as drug certificate; Do not meet the requirements, shall not be purchased.
Article 18 pharmaceutical trading enterprises must have true and complete records of purchasing and selling drugs. The purchase and sale records must indicate the general name, dosage form, specification, batch number, validity period, production enterprise, purchase (sales) unit, purchase (sales) quantity, purchase and sale price, purchase (sales) date and other contents as stipulated by the drug supervision and administration department of the State Council.
Article 19 Drug trading enterprises must sell drugs accurately, and correctly explain the usage, dosage and precautions; The prescription must be checked, and the drugs listed in the prescription shall not be changed or replaced without authorization. Prescriptions with incompatibility or overdose should be refused to be prepared; When necessary, it can be prepared only after being corrected or re-signed by the prescriber.
When selling Chinese herbal medicines, pharmaceutical trading enterprises must indicate the place of origin.
Article 20 Pharmaceutical trading enterprises must formulate and implement a drug storage system, and take necessary measures such as cold storage, anti-freezing, moisture prevention, insect prevention and rat prevention to ensure the quality of drugs.
The storage and distribution of drugs must implement the acceptance system.
Twenty-first Chinese herbal medicines can be sold in urban and rural fairs, except as otherwise provided by the State Council.
Drugs other than Chinese herbal medicines may not be sold in urban and rural fairs, but pharmaceutical retail enterprises holding the Drug Business License may set up outlets in urban and rural fairs to sell drugs other than Chinese herbal medicines within the prescribed scope. Specific measures shall be formulated by the State Council.
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