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NameRequirements for Approval letter of Pharmaceuticals Import Permit
DescriptionThe 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.
CommentsAn 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
Validity From01-01-2016
Validity To09-09-9999
Reference
Technical Code
Agency69
Created Date2020-03-17 02:30:48
Updated Date2020-07-23 03:40:35
StatusActive
Measure TypePermit Requirement
Legal/RegulationMedicines And Related Substances Control Act, 2016
Un Code

Procedures

Displaying 1-1 of 1 result(s).
Procedure NameDescriptionCategoryView Procedure Detail with Relevant Forms
Approval Letter for Pharmaceuticals Import PermitThis process represents the procedure for obtaining a pharmaceutical import permit. One permit is issued for each consignment.ImportView

 

This measure applies to commodity/s
Displaying 111-112 of 112 result(s).
HS CodeDescription
APPLIANCES IDENTIFIABLE FOR OSTOMY USE
WASTE PHARMACEUTICALS
Member Area

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