Licenses library · 698
License to Import Raw Materials for the Production of Registered Drugs
已注册药品生产用原料进口许可证
ໃບອະນຸຍາດນຳເຂົ້າວັດຖຸດິບເພື່ອຜະລິດຢາທີ່ໄດ້ຈົດທະບຽນແລ້ວ
A company or factory that obtains a permit from the Food and Drugs Department. Apply at Food and Drugs Department.
Who needs this
A company or factory that obtains a permit from the Food and Drugs Department.
Documents — first application
| Document | Note |
|---|---|
| Request Letter | to import medical equipment |
| Invoice | 3 copies |
| Packing List | 3 copies |
| Purchase Order (PO) | 3 copies |
| Certificate of Analysis | of imported manufacturing tools |
| Certificate of Good Manufacturing Practice (GMP) |
Legal framework
- Law on Drugs and Medical Products (Amended)
- Notice on the Required Documents for the Application on Import Raw Materials, Packaging, Medicine and Medical Equipments for Manufacturing and Distribution
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
- NO
- Renewal process
- It can be used only once.