Specialty and hard-to-find medicines, supplied worldwide from India
Named-patient, orphan, comparator and shortage medicines from licensed manufacturers, delivered to hospitals, importers, trial sponsors and NGOs with the documents each country requires.
- Quote target 24 to 48 hours
- Licensed buyers and physicians only
- Documents built for your country
- Cold chain with data loggers
Document pack for your destination
Built from the import rules of your country
- Import permit or special-access approval
- Certificate of analysis for the lot
- COPP and GMP certificate
- Commercial invoice and packing list
- Temperature logger file
Who we supply
One supply desk, six kinds of buyer
Each buyer type has its own legal route, verification and documents. Choose yours to see exactly what applies to you.
Hospitals and hospital pharmacies
Named-patient, shortage, orphan and specialty medicines for the patients in your care.
See how it worksBefore a quote we need
Hospital licence and a named pharmacist contact
Importers and distributors
Indian generics and specialty lines in volume, and unlicensed imports under your own permits.
See how it worksBefore a quote we need
Import or wholesale licence, company registration and tax ID
CROs and trial sponsors
Comparators, reference listed drugs and ancillaries with batch, expiry and pedigree control.
See how it worksBefore a quote we need
Company verification and a protocol reference
NGOs, governments and tender bodies
HIV, TB, malaria and essential medicines for programmes and tenders, with quality status per line.
See how it worksBefore a quote we need
Organisation registration and the tender documents
Physicians
Named-patient requests for a patient in your care, quoted to your hospital or another licensed consignee.
See how it worksBefore a quote we need
Your licence number and registering council
Patients and families
We cannot supply you directly, but we can work with your doctor. See how the physician route works.
See how it worksBefore a quote we need
The treating doctor's name and contact
The catalogue, as it stands today
Live counts from our database. Every presentation links to its molecule, its manufacturer and the documents available.
Browse all medicinesHow supply works
From request to delivery in six clear steps
Typical targets from our supply process. Your quote shows the exact lead time for your medicine and your country.
- 01
Request
Send the medicine, quantity and destination. The country rules show the legal route and the documents needed.
Instant - 02
Verification
We verify your organisation and licences and screen the buyer and consignee against sanctions lists.
1 business day - 03
Documents and pharmacist review
For named-patient requests a pharmacist checks the prescription, import approval and consent before the quote.
Within the quote target - 04
Quote
A versioned quote with price, validity, Incoterm, lead time and the list of documents included.
24 h listed, 48 h sourced - 05
Payment
Named-patient and first orders are paid in advance by bank wire. Bank details appear only on your proforma invoice.
Before procurement - 06
Procurement and dispatch
We procure from the licensed source, record batch, expiry and CoA, then ship by medical courier or air cargo.
7 to 10 days, then transit
Services
Built for the hard cases
Unlicensed, scarce, cold-chain or paperwork-heavy medicines, each handled through the regulatory route it needs.
Named-patient supply
Unlicensed and unapproved medicines for an individual patient, through the import route your regulator allows.
Explore the service
Clinical trial comparators
Comparators, reference listed drugs and ancillaries with batch, expiry and pedigree documents for every lot.
Explore the service- Orphan and rare disease medicinesMedicines for rare conditions that are scarce, unregistered or slow to reach your market.
- Shortage supplyEquivalent medicines from India or other markets when local stock of a registered medicine runs out.
- Tenders and NGO supplyEssential medicines for programmes, ministries and NGOs, with the quality status each funder requires shown per line.
- Cold chain logistics2 to 8 °C and frozen lanes with qualified shippers, data loggers and good distribution practice.
- Wholesale exportIndian generics and specialty lines in volume for licensed importers and distributors.
- Regulatory documentsCertificates of analysis, COPP, GMP certificates and export paperwork, organised for your regulator.
Therapy areas
Browse by therapy area
Molecules grouped by clinical area, each with its presentations, manufacturers and supply notes.
Cold chain and logistics
The right lane for every shipment
Temperature, weight and control status decide how a consignment travels. Your quote names the lane, the Incoterm and the transit time.
- 1
Room temperature, up to about 30 kg
Medical courier
- Typical transit
- 3 to 7 days
- Controls
- The courier clears customs, no separate customs agent needed
- 2
Cold chain, small lots
Qualified passive shipper by medical courier or a specialist
- Typical transit
- 3 to 7 days, within the shipper's validated hours
- Controls
- Data logger file linked to the lot
- 3
Cold chain or bulk, larger lots
Air cargo in active containers through a customs agent
- Typical transit
- 7 to 15 days
- Controls
- GDP handling and continuous monitoring
- 4
Controlled medicines
Air cargo only, after a per-consignment export authorisation
- Typical transit
- Not offered at launch
- Controls
- Blocked from online requests
- CIP and DDP quotes include all-risk cargo insurance that covers temperature excursions.
- Your lead time adds up sourcing, Indian export clearance, the destination permit and transit, and the quote shows each part.
- Airline pharma products publish their ranges. Air India Cargo holds −20 to +20 °C and IAG Cargo −20 to +25 °C.
Quality you can check
Every lot traceable, every claim sourced
Specialty medicines leave no room for guesswork. These are the controls behind every quote and every shipment.
- 1Suppliers qualified on their manufacturing licence and GMP certificate before we procure from them
- 2Batch, expiry and certificate of analysis recorded for every lot, with a minimum remaining shelf life on dispatch
- 3Storage and transport under good distribution practice, with temperature data for cold-chain lots
- 4Named-patient files reviewed and signed off by a pharmacist
- 5Complaints, returns, recalls and side effect reports handled through a written procedure
Import guides
What your country requires
Regulator, legal route, documents and typical approval times, verified and dated for each country.
- Brazil
- Regulator
- Brazilian Health Regulatory Agency (ANVISA)
- Typical approval
- ANVISA does not publish a processing time for hospital imports under RDC 488/2021. The gov.br page for exceptional requests filed through SEI gives an average of 30 working days, so plan for several weeks and confirm the current timeline with ANVISA or a Brazilian customs broker.
- Colombia
- Regulator
- National Institute for Food and Drug Surveillance (INVIMA)
- Typical approval
- Neither Decree 481 of 2004 nor the Ministry of Health guidance reviewed sets a processing time for INVIMA authorisations, and INVIMA can ask for missing documents before deciding. Plan for one to several weeks and confirm the current timeline with INVIMA or a Colombian importer.
- Egypt
- Regulator
- Egyptian Drug Authority (EDA)
- Typical approval
- EDA does not publish a processing time for special or individual request approvals. It issues approvals for registered imports within 48 hours and emergency approvals within one working day, so plan 2 to 6 weeks for an unregistered product and longer when a technical assessment or batch testing applies.
- Ethiopia
- Regulator
- Ethiopian Food and Drug Authority (EFDA)
- Typical approval
- EFDA does not publish a processing time for special import authorisations for unregistered medicines. Plan for several weeks and confirm the current timeline with EFDA or a local agent before fixing a delivery date.
- Ghana
- Regulator
- Food and Drugs Authority (FDA Ghana)
- Typical approval
- FDA Ghana states that a clearance permit for a registered product can be processed within one working day after fees are paid. No time is published for special approvals or named-patient permits, so allow one to several weeks and confirm with the FDA.
- Iraq
- Regulator
- Ministry of Health, Directorate of Technical Affairs (with Kimadia and the National Center for Drug Control and Research)
- Typical approval
- The Ministry of Health does not publish processing times. Regular registration was reported at about a year and fast-track temporary registration at about one month in 2021, and no timeline was found for exceptional imports, so plan 1 to 3 months and confirm with the Ministry or a scientific bureau.
- Kazakhstan
- Regulator
- Committee for Medical and Pharmaceutical Control of the Ministry of Health (KMFK), with the National Center for Expertise of Medicines and Medical Devices (NCELS)
- Typical approval
- The import rules give the Committee 3 working days to issue the conclusion once a complete application is filed. The council of doctors, patient consent and regional health authority letter come first and have no published time limit, so plan for 1 to 4 weeks in total.
- Kenya
- Regulator
- Pharmacy and Poisons Board (PPB)
- Typical approval
- Import permits follow the PPB service charter, which the 2026 guideline references without stating times. Compassionate use reviews have published targets of 7 to 30 calendar days, so allow 1 to 4 weeks overall and confirm with PPB.
Trust and transparency
Published as it is verified
Licence numbers link to the issuing registry, and company details appear here once they are confirmed. Nothing on this page is a placeholder.
What we commit to
- Licensed buyers only, and no consumer checkout for prescription medicines.
- Clinical text taken from regulator labels and reviewed by a named professional before it is published.
- A certificate of analysis for every lot we ship, with batch records you can trace.
- Every side effect report reviewed by a pharmacist and forwarded to the marketing authorisation holder.
- Licence numbers published only once verified, each with a link to the issuing registry.
- Our bank details appear only on your proforma invoice, never on the website or in a chat message.
Questions buyers ask first
Short answers. Each service page and import guide goes into more detail.
Do you sell medicines to patients directly?
No. We supply licensed hospitals, importers, distributors, trial sponsors, NGOs and physicians acting for a named patient. Patients and families can start an enquiry, and we then work through the treating doctor, so the quote goes to the doctor's hospital or another licensed consignee.
Which countries can you supply?
We can quote for any destination where a licensed buyer may legally import the medicine, subject to sanctions screening. Each import guide explains the regulator, the legal route and the documents needed, and the request form checks the route for your country.
How fast will I receive a quote?
Our target is 24 hours for medicines in the catalogue and 48 hours for medicines we need to source, counted from the time your request and documents are complete. The quote shows price, validity, Incoterm, lead time and the documents included.
How do I pay?
By bank wire transfer in USD, EUR, GBP, AED or INR. Named-patient and first orders are paid in full before we procure the medicine. Our bank details appear only on the proforma invoice, never on the website or in a chat message.
Which documents come with a shipment?
A commercial invoice, a packing list and a certificate of analysis for each lot, plus the manufacturer's COPP or GMP certificate where your regulator asks for it. Cold-chain shipments include the temperature logger file. The import permit or special-access approval is obtained by you or your local licensed importer.
Can you supply a medicine that is not approved in my country?
Often, yes, through a regulator-approved special-access or named-patient route. The request comes from a licensed party in your country, such as a hospital or an importer, and the import approval must be in place before dispatch. Some products also need an export permission from India's drug regulator.
Do you handle cold-chain medicines?
Yes. Medicines stored at 2 to 8 °C or frozen travel in qualified shippers with a data logger, by medical courier for small lots or by air cargo in active containers for larger lots. The logger file is linked to the lot record.
Do you supply controlled medicines?
Not at launch. Narcotic and psychotropic medicines need a separate export authorisation for every consignment under Indian law, so they are excluded from online requests.
Regulatory and supply updates
A short email when new approvals, shortages or import rules change what buyers can source. No promotions, and you can unsubscribe in one click.
Tell us which medicine you need
Send one line or a full list. You receive availability, a firm quote and the document checklist for your country.
Licensed buyers and physicians only. Patients and families, please start with your doctor.