ExportsAfricaCameroon

Pharmaceutical Manufacturer in India for Cameroonian Importers

Your brand, made at our own WHO-GMP plant in Panchkula, with the DPML registration held in your name

Cameroon imports over 90 per cent of its pharmaceutical needs; imports reached 166.6 billion FCFA in 2023. The importers who do well are the ones whose Indian source answers DPML’s questions, stands up to a site inspection and ships the same quality on the tenth order as on the first. That is the job we do.

  • Our own plant, not a trading house. One WHO-GMP site for tablets, capsules and oral liquids, with GLP laboratories in the next block. DPML queries are answered by the people who made the batch.
  • Artwork and foil printed in-house. Your blister foil and cartons are printed on our own rotogravure unit, so a DPML label change or a re-order never waits on a converter.
  • One container, your whole range. Tablets, capsules, oral liquids and creams from one gate, with 39 products already approved for export to USP and BP monographs.
Supplying Cameroon

Start here

Send us four things and you get feasibility, rate, batch size and lead time in writing.

  1. Products and strengths you want to register
  2. Pack sizes and annual quantity
  3. DPML’s document requirement list
  4. Your artwork, or ask us to prepare it


Email info.vh@vibcare.co.in
Request samples

Or call +91 85660 76607

Why Cameroonian importers work with Vibcare Healthcare

What is different when the manufacturer owns the plant

DPML-ready from the site

Site certificates, product specifications, batch records, certificates of analysis and stability data come from one quality unit, on DPML’s checklist, in the order the assessor asks for them. The plant is open to DPML inspection by appointment.

Documentation that survives an audit

Every batch ships with its certificate of analysis and batch manufacturing record. Written specifications, validated methods and ICH stability data from our own chambers, run at the conditions Cameroon’s climatic zone requires.

Your brand, your artwork, our press

French and English packs with the DPML registration number, batch and expiry printed to your approved artwork; blister and strip foil printed inside the plant on a 4-colour rotogravure unit. Label changes stay on our schedule.

A range, not a product

Anti-infectives, cardiovascular, gastro-intestinal, pain and anti-allergic products from the export list, plus anything from 750-plus approved formulations added against your order, consolidated into one consignment to Douala.

Operators at the ACG AF90T capsule filling machine, Vibcare Healthcare plant
Analyst at the HPLC in the quality control laboratory, Vibcare Healthcare
Manufacturing block at the Vibcare Healthcare plant, Dabkori, Panchkula

From Panchkula to Douala

Road to Nhava Sheva, sea through Suez and the Atlantic; air freight to Douala International Airport

PanchkulaNhava Sheva (JNPT)Douala
IncotermsQuoted FOB Nhava Sheva or CIF Douala, per consignment
PaymentAgreed at proposal stage; letter of credit or bank transfer
Lead timeGiven in writing with the proposal, counted from artwork approval
SamplesOn request against the products you intend to register

What is already in place

Numbers an importer can check

WHO-GMPsite certificate No. 1/182-1Drug-I-2024/10117, FDA Haryana
39products export-approved to USP and BP monographs
22markets supplied, 14 of them in Africa
GLPcertified QC and microbiology laboratories on site

How DPML registration runs with us

You apply; the manufacturer’s part comes from Dabkori

What arrives from Dabkori for your DPML file

  • Notarised power of attorney naming your company as applicant
  • WHO-GMP site certificate, GMP (Revised Schedule M) and GLP certificates
  • Manufacturing licences MLF252023HR000004 and MLF282023HR000005
  • Product specifications and methods of analysis, finished product and raw material
  • Batch manufacturing and packing records, with certificates of analysis
  • Stability data from ICH accelerated and long-term studies in our own chambers
  • Samples of each product for DPML laboratory analysis where required
  • Label, leaflet and carton artwork proofs in French and English, with the registration number and batch details
  • Answers to assessor queries, and the plant open for DPML site inspection
  • Further items on DPML’s checklist as they are asked for
  1. You send the requirement. Products, packs, quantity and DPML’s document list. Confidentiality agreement signed first if you want one.
  2. We answer in writing. Feasibility against the export list and licence, rate, batch size, lead time, and a notarised power of attorney naming your company as applicant.
  3. Dossier and samples. The dossier carries a letter of commitment from the applicant's regulatory pharmacist, countersigned by a pharmacist registered with the Cameroon Order of Pharmacists who acts as the local interlocutor with the DPML. Manufacturer’s documents are supplied in DPML’s format (CTD, in French or English (CEMAC format)), samples shipped where required, assessor queries answered from the site.
  4. First consignment. Artwork approved, batches manufactured and released against specification, and shipped with certificate of analysis and batch documents. Sea freight to Douala through Suez and the Atlantic from India's west-coast ports. The DPML guide gives the National Drug Commission up to 3 months for its opinion and the Minister up to 2 months to decide. Registration validity: 5 years.

The plant behind your brand

Four sections at Dabkori, Panchkula, commissioned in 2023

Tablets — 1.1 billion a year

Two Saral granulation lines, 27- and 37-station Karnavati presses, 48-inch Gansons auto-coater; uncoated, film-coated, enteric, sustained-release, dispersible and bilayer tablets. 334 formulations on the product list.

Capsules — 950 million a year

ACG AF90T automatic filling with a Captech semi-automatic line; powder, pellet and pellet-plus-powder fills, enteric PPI and sustained-release pellets. 69 formulations on the product list.

Oral liquids — 30 million bottles a year

NPM 3 kL manufacturing plant and 6-head filling line; syrups, suspensions, solutions and oral drops in HDPE, PET and glass. 85 formulations on the product list.

Creams, ointments and gels — 40 million tubes a year

NPM manufacturing plant and Pacmac tube filler; creams, ointments, gels, lotions and topical solutions in laminate and aluminium tubes. 108 formulations on the product list.

Packing and printing
Blister and alu-alu machines from Elmach and Rapid-Pack, strip packing from Satellite Engineers, and a 4-colour MMW rotogravure unit printing blister and strip foil inside the plant
Quality control
GLP certified laboratories in a separate block: Shimadzu HPLC, Electrolab dissolution, UV, Thermolab stability chambers running ICH accelerated and long-term studies, and a separate microbiology laboratory with HEPA-filtered laminar air flow

Plant infrastructure

What a DPML inspector sees on site

Layout
Two blocks on a 5-acre site with one-directional material and personnel flow. Block 1: manufacturing, packing, finished goods and dispatch. Block 2: quality control, microbiology, quality assurance, warehouses and administration.
HVAC
57 air handling units from Edgetech serving production and QC, with chillers from Blue Star
Purified water
RO system with SS 316L storage and a continuously circulating distribution loop
Power and utilities
Diesel generator backup of 380 kVA and 62.5 kVA; steam generation and compressed air
Building management
BMS built on ABB, Honeywell and Siemens hardware
Environment and safety
Effluent and sewage treatment plant, fire hydrant and fire safety systems across the site
Certification held
WHO-GMP site certificate No. 1/182-1Drug-I-2024/10117 (FDA Haryana, 24 October 2024), GMP under Revised Schedule M, GLP certificate for the laboratories, manufacturing licences MLF252023HR000004 and MLF282023HR000005, ISO 9001:2015. Product registrations in Cameroon are held by the applicant named in the DPML file.

All 39 export approvals

On the Indian licence, written to USP and BP monographs

Cardiovascular
Amlodipine tablets USP 5 mg and 10 mg · atorvastatin tablets BP 10 mg and 20 mg · bisoprolol fumarate tablets USP 2.5 mg and 5 mg · carvedilol tablets USP 3.125 mg and 6.25 mg · losartan tablets USP 50 mg · propranolol tablets USP/BP 10 mg and 40 mg · rosuvastatin tablets BP 10 mg · telmisartan tablets BP 20 mg
Anti-infective
Azithromycin tablets USP 250 mg and 500 mg · azithromycin oral suspension USP 200 mg · ciprofloxacin tablets BP 500 mg · levofloxacin tablets USP 500 mg · linezolid tablets USP 600 mg · moxifloxacin tablets BP 400 mg · norfloxacin tablets BP 400 mg · rifaximin tablets BP 550 mg
Gastro-intestinal
Esomeprazole gastro-resistant tablets BP 20 mg and 40 mg · omeprazole gastro-resistant capsules BP 20 mg · pantoprazole gastro-resistant tablets USP 40 mg · ranitidine tablets BP 150 mg · ursodeoxycholic acid tablets BP 300 mg
CNS, pain and steroid
Levetiracetam tablets USP 500 mg · pregabalin capsules BP 75 mg · duloxetine delayed-release capsules USP 20 mg · paracetamol tablets BP 500 mg · ibuprofen tablets BP 400 mg · methylprednisolone tablets USP 4 mg
Anti-allergic
Cetirizine tablets BP 10 mg · levocetirizine tablets USP 5 mg · desloratadine tablets USP 5 mg
Metabolic and urology
Metformin prolonged-release tablets BP 1000 mg · tamsulosin modified-release capsules BP 400 mcg

Any other product from the 750-plus approved formulations is added to the export list against your order, with the export approval applied for from FDA Haryana and stability set down for Cameroon’s climatic zone.

Questions Cameroonian importers ask

Before you send a requirement

Who applies to DPML, you or us?

You do. The dossier carries a letter of commitment from the applicant's regulatory pharmacist, countersigned by a pharmacist registered with the Cameroon Order of Pharmacists who acts as the local interlocutor with the DPML. We give you a notarised power of attorney, every manufacturer's document on DPML's checklist, samples for laboratory analysis and answers to assessor queries from the site.

Will DPML inspect your plant?

Regulators may inspect foreign manufacturing sites as part of registration. Ours is a WHO-GMP certified plant commissioned in 2023, with GLP laboratories on site, and it is open to DPML and to you by appointment.

How long until my product is registered and shipped?

The DPML guide gives the National Drug Commission up to 3 months for its opinion and the Minister up to 2 months to decide. Registration validity: 5 years. The manufacturing lead time for your first consignment comes with the proposal, in writing.

Which language do you print the packs in?

French and English, to the artwork you approve, with blister and strip foil printed inside our plant. Dossier documents are supplied in the format DPML uses: CTD, in French or English (CEMAC format).

What is the minimum order?

It follows the batch size of each product. Because tablets, capsules and oral liquids come from one site, a first consignment is usually consolidated across products rather than filled with one.

Which products can you supply straight away?

39 products already approved for export to USP and BP monographs, across anti-infectives, cardiovascular, gastro-intestinal, pain and anti-allergic classes. Anything else on our 750-plus approved formulations is added to the export list against your order.

Send your Cameroon requirement today

Products, pack sizes, annual quantity and DPML’s document list. You will get feasibility, rate, batch size and lead time in writing.

info.vh@vibcare.co.in  ·  +91 85660 76607  ·  Khasra 6/2/2, Kot Road, Village Dabkori, Panchkula, Haryana 134103  ·  Other markets in Africa