Commodity


Chapter
30 PHARMACEUTICAL PRODUCTS

Sub Chapter
3001 Glands and other organs for organo-therapeutic uses, dried, whether or not powdered; extracts of glands or other organs or of their secretions for organo-therapeutic uses; heparin and its salts; other human or animal substances prepared for therapeutic or

Sub Heading
300120 - Antisera, other blood fractions and immunological products, whether or not modified or obtained by means of biotechnological processes

Code
30012000 EXTRACTS OF GLANDS OR OTHER ORGANS OR OF THEIR SECRETIONS

 

Tariffs


Displaying 1-12 of 12 result(s).
Country GroupGroup DescriptionActivityTariff RateUnitValid FromValid To
FULLNON PREFERENTIALImport0kg01-07-201730-06-2018
MFNMOST FAVOURED NATION (WTO)Import0kg01-07-201730-06-2018
COMESACOMESAImport0kg01-07-201730-06-2018
SADCSADC (EXCL. RSA)Import0kg01-07-201730-06-2018
RSARSA (SOUTH AFRICA)Import0kg01-07-201730-06-2018
PORPORTUGALImport0kg01-07-201730-06-2018
BTABOTSWANA TRADE AGREEMENTImport0kg01-07-201730-06-2018
ZIMZIMBABWE TRADE AGREEMENTImport0kg01-07-201730-06-2018
COZCOMESA FREE TRADE AREAImport0kg01-07-201730-06-2018
MOZMOZAMBIQUE TRADE AGREEMENTImport0kg01-07-201730-06-2018
EXCISEEXCISEImport0kg01-07-201730-06-2018
VAT (IMP)IMPORT VATImport0kg01-07-201730-06-2018

 

Measures


Name Type Agency Description Comments Law Validity
Medicine import licences Licensing Requirement Poisons Board of Malawi Any person importing any medicinal product must apply for a product licence. To have an assurance that the port in which the person is importing is a registered port and in order to check the quality of products authorized to enter. Pharmacy, Medicines and Poisons Act (35:01) 31-12-9999

Procedures

Name Description Category View Procedure Detail with Relevant Forms
Application for a medicine importation license. Application for a Medicine Importation License Under Pharmacy Medicines and Poisons Act. Section 35, 36, 37, 38, 38, 39,40,41,66. Procedure View

Measures


Name Type Agency Description Comments Law Validity
Medicine export licences Licensing Requirement Poisons Board of Malawi Any person exporting any medicinal product into malawi must apply for a product licence. To make sure that the manufacturer is able to meet the required medicinal standards. Pharmacy, Medicines and Poisons Act (35:01) 31-12-9999

Procedures

Name Description Category View Procedure Detail with Relevant Forms
Application for a medicine exportation license. Application for a Medicine Exportation License Under Pharmacy Medicines and Poisons Act. Section 35, 36, 37, 38, 38, 39,40,41,66. Procedure View

Measures


Name Type Agency Description Comments Law Validity
Exemptions in medicine import licences Licensing Requirement Poisons Board of Malawi The importation of a medicinal product by any person for administration to himself or to any persons who are members of his household, or the importation of a medicinal product where it is specially imported by or to the order of a medical practitioner or dentist for administration to his patient can be made without a licence provided that in either case the quantity imported is not too much. This is mainly done in cases where a patient is stabilised on a certain brand of medication not available in Malawi and where the doctor advises that such medication should continue to be administered to the patient. Pharmacy, Medicines and Poisons Act (35:01) 31-12-9999

Procedures

Name Description Category View Procedure Detail with Relevant Forms
Application for an exemption to medicine license. Application for an Exemption to Medicine License Under Pharmacy Medicines and Poisons Act. Section 36 (g). Procedure View

Measures


Name Type Agency Description Comments Law Validity
Containers, package, and identification of medicinal products Labelling Requirement Poisons Board of Malawi All medicinal products for the purpose of selling or supplying must be in a container or package and properly labelled. Identifies the product to know the type medicine; Offers guidance in use and storage of the product. Pharmacy, Medicines and Poisons Act (35:01) 31-12-9999

Measures


Name Type Agency Description Comments Law Validity
Application for registration and retention of registration of medicinal products Registration Requirement Poisons Board of Malawi Every applicant must, without delay, inform the Board either before or after the registration of a medicinal product whether the medicinal product is to be imported as a finished product into Malawi, or re-labelled. or repackaged or dealt with in any other manner, in Malawi. This applies in countries where medicine ingredients are found in several countries and medicines are shipped to them at different levels of manufacturing. Pharmacy, Medicines and Poisons Act (35:01) 31-12-9999

Procedures

Name Description Category View Procedure Detail with Relevant Forms
Application for registration of medicinal products. Application for Registration of medicinal Products Under Pharmacy, Medicines and Poisons (Fees and Forms) Regulations. Rule 13(3) and (4). Procedure View

Measures


Name Type Agency Description Comments Law Validity
Importation of medicinal products with less than one-half of shelf-life Prohibition Poisons Board of Malawi No person can, without the prior written approval of the Board, import into Malawi any medicinal product which has less than one-half of its shelf-life remaining upon arrival in Malawi. Malawi should not be a dumping ground for medicines and to avoid exploitation of donors sending too much medication in Malawi. "package", in relation to any medicinal products, means any box, packet or other article in which one or more containers of the medicinal products are or are to be enclosed, and where any such box, packet or other article is or is to be enclosed in one or more other boxes, packets or articles in question, the collective number thereof; Pharmacy, Medicines and Poisons Act (35:01) 31-12-9999