Commodity

Chapter

30 Pharmaceutical products

Sub Chapter

3002 Blood, human or animal; prepared for therapeutic, prophylactic, diagnostic uses; antisera and other blood fractions; vaccines, toxins, cultures of micro organisms, similar products (not yeasts)

Sub Heading

300230 VACCINES FOR VETERINARY MEDICINE

Code

3002300000 VACCINES FOR VETERINARY MEDICINE

Tariffs

Displaying 1-6 of 6 result(s).

Country Group	Group Description	Activity	Tariff Rate	Unit	Valid From	Valid To
CDG	Customs Duty General	Import	FREE	KG	30-03-2020	31-12-9999
EU-PREF	EU Preferential Rate	Import	FREE	KG	30-03-2020	31-12-9999
EFTA-PREF	EFTA Preferential Rate	Import	FREE	KG	30-03-2020	31-12-9999
SADC-PREF	SADC Preferential Rate	Import	FREE	KG	30-03-2020	31-12-9999
MERC-PREF	MERCOSUR - Preferential Rate	Import	FREE	KG	30-03-2020	31-12-9999
VAT	Value Added Tax	Import	15%	KG	30-03-2020	31-12-9999

Measures

Name	Type	Agency	Description	Comments	Law	Validity
Requirements for Approval letter of Pharmaceuticals Import Permit	Permit Requirement	Ministry of Health	The Ministry of Health is responsible for authorizing the importation of pharmaceuticals and only authorized pharmaceutical products will be permitted to be imported (or exported) into (or out of) the country.	An application for issue of an import permit shall state, for each medicine to be imported at least the following: i. Generic name or International Non-proprietary Name (INN) ii. Trade name or proprietary name; if any iii. Strength and dosage form iv. Name and strength of the Active Pharmaceutical Ingredient (API) v. Total quantity to be imported vi. Name and address of the supplier/importer vii. Name and address of the manufacturer viii. Country of origin ix. Route of entry x. Expected date of arrival	Medicines And Related Substances Control Act, 2016	09-09-9999

Procedures

Name	Description	Category	View Procedure Detail with Relevant Forms
Approval Letter for Pharmaceuticals Import Permit	This process represents the procedure for obtaining a pharmaceutical import permit. One permit is issued for each consignment.	Import	View

Measures

Name	Type	Agency	Description	Comments	Law	Validity
Import Permit For Pharmaceuticals	Permit Requirement	Ministry of Health	Prior to making an application for an Import Permit, the Importer must be registered and approved with the Ministry of Health. This is a separate process of application and registration under the Pharmaceutical Department and which involved the Medicine Regulatory Unit undertaking inspection of the Importer premises.Only those products on the list associated with the permit can be imported by the Importer. If the item is not on the approved list then the importer must apply for the addition of the new product.	There is no limit on the number of consignments or volume of pharmaceutical products that can be imported against the permit, provided the products is approved under the permit.	Medicines And Related Substances Control Act, 2016	09-09-9999

Measures

Name	Type	Agency	Description	Comments	Law	Validity
Import permit for veterinary drugs and medicinal substances	Permit Requirement	Department of Veterinary and Livestock Services	The importer is required to acquire a veterinary import permit from regional veterinary offices issued by a veterinary officer.	An import permit will only be issued for veterinary drugs and medicinal substances listed for importation and use in Eswatini	Guidelines for National Veterinary Services, 2013	09-09-9999

Measures

Name	Type	Agency	Description	Comments	Law	Validity
Registration Requirement of Pharmaceuticals Importers	Registration Requirement	Ministry of Health	An applicant must fulfill the following requirements when registering to be an Importer of Pharmaceuticals	1. A full time responsible pharmacist (with at least 5 years clinical/retail pharmacy experience) to supervise the pharmaceutical establishment must be engaged 2.The proposed premises for the pharmaceutical establishment must be inspected and approved by the Ministry 3. The pharmaceutical establishment is expected to register with the Ministry as an importer of Medicines using the relevant document (only applicable if the retail pharmacy intends to import medicines) 4. The company must familiarize itself with the Medicines and Related Substances Control Act of 2016, and relevant regulations and any other legislation, regulations and guidelines that relate to the business of pharmaceutical establishments in the country.	Medicines And Related Substances Control Act, 2016	09-09-9999