| Name | A quality analysis certificate is required for imported medical products. |
|---|---|
| Description | Imported medical product must obtain a quality analysis certificate from the National Food and Drug Administration or from an approved domestic or foreign laboratory recognized by the Ministry of Health. |
| Comments | to ensure the quality, safety, and effectiveness of consumers. |
| Validity From | 2016-06-16 |
| Validity To | 9999-12-31 |
| Reference | 52 of Law 85/NA, Clause II of Notification 2660 |
| Measure Type | TBT |
| Agency | Ministry of Health |
| Legal Document | - Notification on the Documents to Request for Import License of Raw Materials, Container Equipment, Drug, and Medical Equipment for Production and Contribution No. 2660/16.FDD, dated 16 June 2016 - Law on Drugs and Medical Products (Amendment) No.07/NA, Dated 10 March 2026 |
| UN Code | B83 |
Procedures
| # | Procedure Name | Description | Category | View Detail |
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Forms
| # | Title | Description | Issued By | File |
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Commodity/s
| # | HS Code | Description |
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Step-by-Step Guide
| # | Process name | Process short name | Activity |
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