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Import Permit (Controlled Chemical)
进口许可（受控化学品）
ໃບອະນຸຍາດນຳເຂົ້າ (ສານເຄມີຄວບຄຸມ)
Any individuals or organizations that intend to import for use, production, or distribution of controlled chemicals 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 use, production, or distribution of controlled chemicals must obtain approval from the Ministry of Health at the time of actual importation.
Requirements
- Any authorized individuals or authorized organizations that carry out the production, import, export, distribution, purchase, transportation, a transit of general chemicals to use in food and drug from the Ministry of Health.
Documents — first application
| Document | Note |
|---|---|
| Application Form for Import Permit of Controlled Chemical | |
| Purchase Order | |
| Invoice | |
| Packing List | |
| Import Authorization of Controlled Chemicals | |
| Copy of Related Registration Certificates and other Permits | such as Enterprise Registration Certificate, Business Operating License and Certificate of Factory Establishment |
| Sample of Import Permit (Controlled Chemical) | download to see the sample of Import Permit for Controlled Chemical |
Legal framework
- Law on Drugs and Medical Products (Amended)
- Order on the Management of Narcotics and Psychotropic Substances
- Order on the List of Narcotics and Psychotropic Substances
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
- - This permit is valid from the signing date until 31 December of that year. - It does not need to renew the import authorization. In case there is no importation during the specified period the import authorization will be eliminated.
Additional comment
- Before import-export-transit of the controlled drugs the authorized importer must obtain an import authorization from the Ministry of Health. - The import company must declare the import authorization 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 authorization.