Commodity
Chapter
30 Chapter 30 - Pharmaceutical products
Sub Chapter
3005 Wadding, gauze, bandages and similar articles (for example, dressings, adhesive plasters, poultices), impregnated or coated with pharmaceutical substances or put up in forms or packings for retail sale for medical, surgical, dental or veterinary purposes.
Sub Heading
300590 - Other:
Code
30059090 - - Other
Tariffs
Displaying 1-3 of 3 result(s).
| Country Group | Group Description | Activity | Tariff Rate | Unit | Valid From | Valid To |
| CD (MFN) | Customs Duty (MFN) | Import | 8 | kg | 01-09-2016 | 31-12-9999 |
| VAT | Value Added Tax | Import | 10 | kg | 01-01-2012 | 31-12-9999 |
| ATIGA | Special Tariff for ASEAN Trade in Goods Agreement | Import | 0 | kg | 01-01-2017 | 31-12-2017 |
24953526162692
Measures
| Name |
Type |
Agency |
Description |
Comments |
Law |
Validity |
|---|
| Import of veterinary drugs requires permission |
Technical Measures |
Ministry of Agriculture and Rural Development |
Any veterinary drug without CFS or not included in the List of veterinary drugs permitted for sale in Vietnam shall be imported in following cases:
a) Materials used for manufacture of veterinary drugs with CFS;
b) Samples used for study, testing, laboratory diagnosis, testing, or registration for sale;
c) Chemical standards used for veterinary diagnosis or testing; veterinary drugs displayed in trade fairs, exhibitions or used for prevention and treatment for precious and rare animals;
d) Medical aid of international organizations and types of other non-commercial imports;
dd) Prevention and treatment of urgent epidemic diseases, disaster recovery. |
Importers of vaccines, biological preparations, microorganisms with CFS in Vietnam or included in the List of veterinary drugs permitted for sale in Vietnam must obtain an approval of Department of Animal Health in writing and subject to/required to undergo quality inspection as prescribed |
Circular 13/2016/TT-BNNPTNT dated June 2, 2016 on veterinary drug management |
31-12-9999 |
Procedures
Measures
| Name |
Type |
Agency |
Description |
Comments |
Law |
Validity |
|---|
| This measure imposes testing requirement for pharmaceutical products which include conditions on testers (inspector with appropriate analytical skills), venue for sampling and sampling equipment |
Inspection Requirement |
Ministry of Health |
Stipulating condition for:
1. conditions on testers
2. venue for sampling
3. sampling equipment |
1. conditions on testers: The Tester must be an inspector or a specialized quality control inspector or a member of the inspection team set up by the agency in charge of State management and inspection of drug quality; have knowledge of drug analysis or testing, firmly grasp legal documents on drug quality management, legal procedures and sampling techniques; must be technically trained and regulated, and must wear appropriate protective clothing when sampling.
2. venue for sampling: This shall be done in a separate area meeting the hygienic requirements (clean grade) and technical requirements of each sample (temperature, humidity, light, ...), avoiding the risk of contamination, cross-contamination of the quality of samples taken as well as the remaining drug after sampling.
For sterile materials, sampling should be carried out in a clean, sterile area
3. sampling equipment
Samplers and sample containers must be made of inert materials appropriate to the characteristics of each type, ensuring that they do not affect the quality of the samples and do not put impurities into contaminated samples or cross contamination. for samples as well as to ensure the safety of samplers (Refer to Appendix 2) |
Circular 04/2010/ TT-BYT guiding drug sampling for quality assurance issued by the Ministry of Health |
31-12-9999 |
Measures
Measures
Measures
