Markets supplied by Vibcare Healthcare, shown in blue. India in navy.
Pharmaceutical Exports from India
WHO-GMP certified manufacturer supplying 22 markets from Panchkula
Vibcare Healthcare exports tablets, capsules and oral liquids from its own WHO-GMP certified plant at Dabkori, Panchkula. 39 products are approved for export to USP and BP monographs, and 22 markets across Africa, Asia and Latin America are supplied today. Registration documentation, stability data and export packing are handled at the site.
Pharmaceutical exports, by the numbers
What is already on the licence for export
Markets supplied
22 countries, grouped by region and regulatory bloc
Africa
West Africa: Nigeria, Ghana, Côte d’Ivoire, Benin, Mali, Burkina Faso
East Africa: Kenya, Tanzania, Uganda, Ethiopia
Southern Africa: Zimbabwe, Zambia
Central Africa: Cameroon
Asia
South Asia: Nepal, Bhutan, Afghanistan
Central Asia: Uzbekistan, Tajikistan
ASEAN: Myanmar, Philippines
West Asia: Yemen
Latin America
Central America: El Salvador
Registration in further Latin American markets is taken up against a confirmed importer and dossier requirement.
Export approvals on the licence
39 products written to USP and BP monographs: 34 tablets, 4 capsules, 1 oral suspension
A product not on this list can be added: the export approval is applied for from FDA Haryana against your market and monograph, and stability is set down in our own chambers for the climatic zone of the market.
Documentation for registration
What travels with a dossier and with every consignment
Site documents
WHO-GMP site certificate No. 1/182-1Drug-I-2024/10117, GMP (Revised Schedule M) and GLP certificates, manufacturing licences MLF252023HR000004 and MLF282023HR000005, ISO 9001:2015. Site master file and further certificates against the regulator’s requirement list.
Product documents
Specifications, method of analysis, batch manufacturing and packing records, certificates of analysis, and stability data from ICH accelerated and long-term studies in our own chambers.
Dossier support
Documentation in the format the target regulator uses, prepared with your registration agent, with queries from the assessor answered from the site.
With every consignment
Certificate of analysis, packing list, batch details and the shipping documents your customs and regulator require.
Packing for export
Language, artwork and shipping
How registration and supply run
Six steps from enquiry to repeat consignment
- Enquiry. Country, products, pack sizes, annual quantity and the regulator’s requirement list.
- Feasibility and proposal. Products checked against the export approvals and the licence; rate, batch size, lead time and documentation scope in writing.
- Dossier. Product and site documents prepared in the regulator’s format, with your registration agent.
- Registration. Assessor queries answered from the site; samples and stability updates supplied as asked.
- First consignment. Artwork approved, batch manufactured, released against specification and shipped with its certificates.
- Repeat supply. Consignments scheduled against your forecast, with stability commitments maintained for the market.
Questions importers ask
Before you send a requirement list
Which countries do you currently export to?
22 markets across Africa, Asia and Latin America: Nigeria, Ghana, Côte d’Ivoire, Benin, Mali, Burkina Faso, Kenya, Tanzania, Uganda, Ethiopia, Zimbabwe, Zambia, Cameroon, Nepal, Bhutan, Afghanistan, Uzbekistan, Tajikistan, Myanmar, the Philippines, Yemen and El Salvador.
Which products are approved for export?
39 export approvals are on the licence, written to USP and BP monographs: 34 tablets, 4 capsules and 1 oral suspension, across cardiovascular, anti-infective, gastro-intestinal, CNS and pain, anti-allergic and metabolic products. The full list is on the product list PDF.
Can you register a product that is not on the export list?
Yes. A new export approval is applied for from the Food and Drugs Administration, Haryana against a confirmed market and monograph, and the timeline is given with the proposal.
Which documents do you supply for registration?
Certificates of analysis, batch manufacturing records, the WHO-GMP site certificate, GMP and GLP certificates, manufacturing licences, stability data and the documents on the importer’s registration requirement list. Certificate requirements differ by regulator and are agreed at the proposal stage.
Do you provide stability data for tropical markets?
Yes. ICH accelerated and long-term studies run in our own stability chambers, with conditions set to the climatic zone of the target market.
Can the pack be printed in our language?
Yes. Cartons, labels and shippers are printed to your artwork in the language the regulator requires, and blister and strip foil is printed inside the plant on our own rotogravure unit.
What is the minimum order for export?
It follows the batch size for the product, which comes with the proposal. Consignments are usually consolidated across products for a container or an air shipment.
Which port do you ship from?
Sea freight moves through Nhava Sheva (JNPT) or Mundra, and air freight through Delhi. Terms and lead times are quoted per consignment.
Talk to us about supply to your market
Send the country, the products, the pack sizes 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
