Trade Export Process Ghana : ghanastradinghub.gov.gh

Organisation : Ghana Trading Hub
Facility : Trade Export Process
Country : Ghana

Homepage : https://www.ghanastradinghub.gov.gh/
Terms & Conditions : https://www.statusin.org/uploads/26706-ExportProcess.pdf

Trade Export Process :

Export Registration Process :
** FDA Exporter Registration

Related : Trade Import Process Ghana : www.statusin.org/26703.html

** FDA Export Product Registration
i. Registration of Locally Manufactured Drug Products
ii. Registration of Locally Manufactured Food Products

** GEPA Export Registration
** GEPA ETLS Product Registration
** GSA Exporter Registration

** GSA Fish Facility Registration
** NACOB Exporter Registration
** PPRSD Exporter Registration

** VSD Exporter Registration
** GNCC Exporter Registration
** GPHA Business Registration

License /Permit/ Certificate/Other Processes :
** FDA Permit Application for Export Clearance
** FDA Permit Application for Certificate of Manufacture and Free Sale
** GSA Product Export Certification

** GSA Fish Export Certification
** PPRSD Application for Phytosanitary Certificate
** PPRSD Wood Packaging Materials (ISPM No 15)

** PPRSD Application for Export Health Certificate
** GNCC Application for Certificate of Origin
** MOTI Permit for Exportation of Non-Ferrous Scrap Metals

** GPHA Export Receipt
** EPA Export Permit
** Export of Goods from Free Zone

** Export for Home Consumption
** Ex-Warehousing Process
** Re-export from the Warehouse

Good Declaration :
** NACOB Export Declaration
Goods Inspection :
** FDA Export Inspection

Clearance :
** Direct Export
** Parcel Post

Cargo Handling :
** Loading of General Cargo/Break bulk
** Loading of RORO Cargo
** Loading of Containerized Cargo
** Loading of Dry Bulk Cargo

Vessel Management :
** Vessel Sailing / Departure

Payment Method :
** Open account
** Letter of credit
** Bill of Collection

Transit Processes :
** NACOB Re-Exportation Permit
** Application for Transit Clearance
** Receiving and Delivery of Loaded Trucks
** Delivery of Vehicle
** Application for transit clearance
** Transit Cargo Registration
** Transhipment

Import Procedure :
1. The Importer completes the registration form, writes an application letter to the CEO Food and Drug Authority stating the intent to register as an importer for Food or other product
2. The Importer pays importer’s registration fees and submits the application Letter and the filled registration form to the Client Service

3. The Client Service Officer receives application; perform documentary check to ensure submitted application meets the minimum requirement. If satisfactory, application is forward to the right division

4. The division receives the application and inspect the premises to ascertain the suitability of the premises for the intended application
5. The application is either approved or rejected on the basis of compliance to the requirements.

Customs Procedures Code :
** Grants and Aids Code: 40A00
** Direct Home Consumption Code: 40D01
** Certified entry following short landing Code: 40D03
** Fish Caught by Ghanaian Registered Vessels in Ghanaian Waters Code: 00N01

** Re-export following warehousing Code: 37X00
** Transit of Petroleum Products from Bond Code: 89R01
** Direct Entry into Ship’s Stores Code: 90S00
** Direct Entry Into Free Zone Code: 90Z00

Contact Address :
Ghana Revenue Authority (Customs Division)
P.O.box 68
HQ
Accra,Ghana.
Tel : +233 242 435 663
Fax : +233-(0)302-681163
Email 1 : support AT ghanastradinghub.gov.gh
Email 2 : support AT ghanastradinghub.com

Functions of the Authority :
a. Ensure adequate and effective standards for food, drugs, cosmetics, household chemicals and medical devices;
b. Monitor through the District Assemblies and any other agency of State compliance with the provisions of Part 6,7 and 8 of the Public Health Act,2012 (ACT 851);

c. Advise the Minister on measures for the protection of the health of consumers;
d. Advise the Minister on the preparation of effective Regulations for the implementation of Part 6,7 and 8 of the Public Health Act,2012 (ACT 851);

e. Approve the initiation and conduct of clinical trials in the country;
f. Perform any other functions that are ancillary to attaining the objects of the Authority