Pharmaceutical Export
Full-container and consolidated shipments with the complete document set — invoice, packing list, CoA, CoO, MSDS — prepared in parallel with production, not after it.
284,047 positions — 21 therapeutic categories and 12 dosage forms, documented.
CoA with every batch. Full export documentation handled end-to-end.
One supplier accountable from your first inquiry to delivery at your door.
No obligation. Reply within 1 business day. Your requirement stays confidential.
284,047 positions with composition, strength, pack size and manufacturer — in your inbox.
One email, with the catalogue attached — no newsletter, no follow-up sequence.
RK Pharma is a pharmaceutical distribution and international healthcare supply company, dedicated to connecting trusted medicines and healthcare products with pharmacies, hospitals, distributors and institutional buyers around the world.
We combine a broad, organised product portfolio with responsive, transparent service — covering sourcing, documentation, and delivery — so our partners can rely on us across the entire supply chain.
Recurring supply with price stability across orders, priority allocation when stock is tight, and marketing support materials for your local registration process.
Tender-ready documentation packs, delivery scheduling built around your procurement cycle, and a dedicated account contact for recurring requirements.
The fast-moving range in one order — mixed SKUs, no rigid minimums per product line, reliable replenishment lead times.
Eligibility and compliance documentation prepared to tender requirements, capacity to fulfil large volumes on schedule.
Eight buyer problems we close on every single order.
No coordinating three vendors for one shipment. We own sourcing, documentation and delivery end-to-end, and one person answers for your order.
CoA, CoO, packing list, MSDS — issued with every shipment, matched to the invoice line by line.
Rework and demurrage caused by paperwork are not your problem.
Quotation within 24 hours on business days. Status update at every stage of your order — without having to ask for it.
If a molecule or strength is not available for your market, you hear it on day one — not after the PO. No silent substitutions, ever.
Transparent, itemised quotations. Price stability across repeat orders.
Volume terms that reward loyalty instead of punishing new buyers.
Factory credentials shared under NDA during onboarding.
Every manufacturer in our network is WHO-GMP certified; selected sites hold EU-GMP and US FDA approvals.
Trial consignments for new partners, mixed-SKU orders for wholesalers, full production batches for tenders — structured to your volume, not ours.
Regulatory queries, reorders, documentation requests for local registration — the relationship continues after delivery.
92% of our buyers reorder.
Because "contact us for details" is where trust goes to die.
First order comes with a dedicated onboarding manager — walkthrough of documentation, packaging specs and logistics.
Every claim on this page is backed by a document we can show you.
IEC 0306019421
20B/21B-MH-2019-004821
27AABCR1234K1ZP
U46497MH2018PTC312004
Member — Pharmexcil (Pharmaceuticals Export Promotion Council of India), Membership No. PXL-114076
Procurement Manager, distributor, West Africa
Recurring orders since 2021
The documents arrived before the container did — CoA, CoO, packing list, everything matched line by line. Customs cleared in two days. With our previous supplier that was three weeks of back-and-forth.
Head of Supply, hospital group, Middle East
Buyer since 2022
We sent a requirement for 14 molecules for a hospital group tender. They quoted in a day, flagged two items that would not pass our regulator, and suggested registered alternatives. That honesty is why we stayed.
Managing Director, wholesaler, Southeast Asia
Recurring orders since 2022
Trial order of 6 cartons in 2022, three containers a quarter now. Prices held stable across the whole period, and when azithromycin went into global shortage, they still filled our allocation.
Browse by therapeutic category or by dosage form — find what you need however you think about it.
The counts are the whole catalogue: 284,047 positions, of which 275,456 sit in the 21 therapeutic categories above. The remaining 8,591 are general, OTC and personal-care lines (7,395) and 1,196 rows the source data carries without a composition. Every entry — composition, strength, pack size, manufacturer, regulatory status and export availability — is shared with partners on request.
The record below is the Azithral 500 Tablet — one entry shown as a specimen of the structure we maintain for every catalogue item.
Entry-specific records are shared with partners on request, under confidentiality where required.
Documentation travels with every shipment.
Certificate of Analysis · Certificate of Origin · Packing List · MSDS
From a single sourcing request to recurring institutional supply.
Full-container and consolidated shipments with the complete document set — invoice, packing list, CoA, CoO, MSDS — prepared in parallel with production, not after it.
Send any molecule, strength or brand — listed or not. We locate it through our manufacturer network within 5 business days and come back with availability and price.
Recurring supply programmes with reserved stock, price stability across the contract term and quarterly volume reviews.
Delivery windows scheduled around your procurement calendar. Cold-chain items shipped with temperature logs.
Eligibility documentation, bid-support paperwork and scheduled fulfilment for institutional and government procurement.
Building a formulary entry for your market? We map manufacturers, compare dossiers and negotiate on your behalf — you see the shortlist, not the noise.
Quality is what the paper proves. Ours always does.
Every batch is checked against specification before dispatch — physical verification, shelf-life window and packaging integrity. Minimum 24 months shelf life on export lots.
Licences and certifications shared during onboarding — not after you have committed. We confirm export eligibility for your destination market before accepting the order.
Product-level dossiers, CoA per batch and regulatory support documents issued to order and destination.
Batch numbers traced from your invoice back to the manufacturing line. Any query answered with documents within 48 hours.
Chamber-attested CoO, notarised documentation where the destination requires it, and document pre-checks against importer declarations.
Export-grade cartons, palletisation to destination standard, language-specific labels on request.
Export documents issued with each shipment, as applicable to the order and the destination market.
Prescription products carry the appropriate professional-use notice, and no therapeutic claim is made beyond approved product information. Certification and licensing documentation is shared with partners as part of the onboarding process.
Every step has a deadline. We put it in writing.
You send the molecule, strength, dosage form and destination market — we confirm scope and feasibility.
Response within 24 hours
We source against your requirement and return a transparent, documented quotation.
Quote within 1–3 business days
Order terms confirmed; export, regulatory and customs documentation prepared and shared.
Document pack within 5 business days of confirmation
Export-ready packing and labelling, dispatched with full shipment documentation.
7–14 days stock items · 21–35 days production
The ten we are asked most, answered without a sales call.
USD 1,000 per order or 100 units per SKU. For first-time partners we accept trial consignments from USD 500 — we would rather earn the second order than force the first.
Within 24 hours on business days for catalogue items, 1–3 business days for sourcing requests outside the catalogue. If a product is unavailable for your market, you will know that within the same timeframe.
T/T advance or LC at sight for new partners. Repeat partners qualify for 30-day credit terms after three completed orders.
We currently serve buyers across 38 countries in North America, Europe, Asia, Africa and Australia. Send your destination market and we will confirm export eligibility and any registration requirements before you commit.
Every shipment travels with: commercial invoice, packing list, Certificate of Analysis (batch-specific), Certificate of Origin (chamber-attested), MSDS where applicable, and Free Sale Certificates on request.
Yes — reference samples are dispatched against your courier account, typically within a week of request.
Every manufacturing partner holds WHO-GMP certification; selected sites additionally hold EU-GMP and US FDA approvals. Factory credentials and audit summaries are shared under NDA during onboarding.
Yes — custom sourcing is one of our core services. Send the molecule, brand or composition and we will map availability across our manufacturer network within 5 business days.
Yes. We prepare eligibility and bid-support documentation and structure scheduled fulfilment for institutional and government procurement. Our tender record includes a 480,000-unit supply contract completed in 26 days.
Temperature-sensitive items ship in validated cold-chain packaging with loggers, and temperature reports are shared with the shipment documents.
Send a requirement today — a documented quotation is in your inbox within 24 business hours.