| Name | Registration or Notification Requirements for Drug Exports |
|---|---|
| Description | Legal entities and organizations exporting medicines must register or notify the relevant authorities by providing product details, including the medicine name, ingredients, dosage form, strength, packaging, source, and other relevant information. This is to ensure proper management, legal compliance, product quality, efficacy, and consumer safety. |
| Comments | To ensure the safety, efficacy, and quality of disease treatment |
| Validity From | 2025-08-25 |
| Reference | Article 53 of Law 85/NA |
| Measure Type | Registration Requirement |
| Agency | Ministry of Health |
| Legal Document | - Law on Drugs and Medical Products (Amendment) No.07/NA, Dated 10 March 2026 |
| UN Code | P12 |
Procedures
| # | Procedure Name | Description | Category | View Detail |
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Forms
| # | Title | Description | Issued By | File |
|---|
Commodity/s
| # | HS Code | Description |
|---|
Step-by-Step Guide
| # | Process name | Process short name | Activity |
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