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Import-Export-Transit Permit of Narcotic Used in Medicine

医药用麻醉品进出口过境许可

ໃບອະນຸຍາດນຳເຂົ້າ-ສົ່ງອອກ-ສົ່ງຜ່ານ ຢາເສບຕິດທີ່ນຳໃຊ້ໃນທາງການແພດ

Any individuals or organizations that intend to: - Import for production, distribution or possession of narcotics - Export - Transit Must obtain approval from the Ministry of Health at the time of actual importation Apply at Food and Drugs Department.

Who needs this

Any individuals or organizations that intend to: - Import for production, distribution or possession of narcotics - Export - Transit Must obtain approval from the Ministry of Health at the time of actual importation

Requirements

  1. Pharmaceutical factory and Import-Export of Pharmaceutical company which has been duly registered with the conditions that can import-export and distribution
  2. Pharmaceutical store class I and II which has been duly registered with the conditions that can retail in accordance with doctor’s prescription
  3. State hospital at a central and local level or private hospital with a license in accordance with condition that can distribute or retail by a pharmacist as per doctor’s prescription.

Documents — first application

Document Note
Purchase Order
Invoice
Packing List
Import Authorization Copy
Certificate of Drug Registration
Certificate of Pharmaceutical Product (CPP)
Certificate of Analysis

How to submit

Means of presentation
At the Authority Offices
Address of authority
Food and Drugs Department, Ministry of Public Health
Processing time
3

Validity and renewal

Has an expiry date
YES
Renewal process
- ໃບອະນຸຍາດນີ້ ມີອາຍຸນັບແຕ່ມື້ລົງລາຍເຊັນຈົນເຖິງວັນທີ 31 ທັນວາຂອງປີນັ້ນໆ. - ບໍ່ມີການຕໍ່ອາຍຸໃບອະນຸຍາດນຳເຂົ້າຕົວຈິງ. ໃນກໍລະນີບໍ່ມີການນຳເຂົ້າຕາມໄລຍະເວລາທີ່ກຳນົດໄວ້ ຖືວ່າໃບອະນຸຍາດດັ່ງກ່າວຈະຖືກລົບລ້າງ.

Additional comment

- Before import-export-transit of the narcotic the authorized importer must obtain an import authorization from the Ministry of Health. - The import company must declare the import permit and relevant documents to the food and drug authority at the checkpoint each time. In case there is any change in the import authorization the import company must return the original of the import authorization to the Food and Drug Department in order to amend such import permit.

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