Pharmaceutical Exports to Africa from India
21 markets across West, East, Southern and Central Africa. Written rate per pack against your product list.
African markets we can register and supply in, shown in blue.
Africa is the largest of the three regions on our export list: 21 of the 38 markets are here. Products are registered through the importer with the national regulator, and in the East African Community and the SADC ZAZIBONA procedure a single assessment can be shared across several countries. Stability studies run in our own chambers at the conditions the market’s climatic zone requires.
Sub-regions and regulatory blocs
How registration is approached in each part of the region
What we make for the region
From the 39 export approvals and the four sections of the plant
Tablets
34 export approvals: cardiovascular, anti-infective, gastro-intestinal, CNS and pain, anti-allergic and metabolic products to USP and BP monographs.
Capsules
Omeprazole gastro-resistant, duloxetine delayed-release, pregabalin and tamsulosin modified-release capsules.
Oral liquids
Azithromycin oral suspension USP; further syrups and suspensions registered against a confirmed importer.
Documentation
Site and product documents, stability data for the climatic zone, and packing in the regulator’s language. Details on the exports page.
Questions importers ask
Before you send a requirement list
Which African countries do you supply?
Nigeria, Ghana, Côte d’Ivoire, Benin, Mali and Burkina Faso in West Africa; Kenya, Tanzania, Uganda and Ethiopia in East Africa; Zimbabwe and Zambia in Southern Africa; and Cameroon in Central Africa.
Do you provide French-language dossiers and packs?
Yes. Packs, leaflets and the documentation the regulator asks for are prepared in French for the francophone markets, working with your registration agent.
Is your stability data suitable for African markets?
Yes. Studies run in our own chambers at the conditions of the market’s climatic zone, including the hot and humid zone IVb conditions most of the continent falls under.
Can one registration cover several countries?
Partly. The EAC joint assessment and the SADC ZAZIBONA procedure share one assessment across member countries, but each national regulator still issues its own registration.
Which documents do you supply for NAFDAC or Ghana FDA registration?
Site documents, product specifications and methods, batch records, certificates of analysis and stability data, plus the items on the regulator’s checklist, agreed at the proposal stage.
Talk to us about supply to Africa
Send the country, the products and the regulator’s requirement list. You will get feasibility, rate, lead time and the documentation scope in writing.
info.vh@vibcare.co.in · +91 85660 76607 · Khasra 6/2/2, Kot Road, Village Dabkori, Panchkula, Haryana 134103
