PharmaOneLink

Find the manufacturer,
not the middleman

Find the pharmaceutical manufacturer behind any molecule or brand and contact them directly.

Create an account See pricing
28,296ManufacturersDrawn from official medicine registers, with each company's own website where one is on file.
21,762MoleculesDeduplicated active ingredients, searchable by INN or brand name.
100CountriesWhere the manufacturers are based.

What PharmaOneLink is

A directory of pharmaceutical manufacturers for buyers, importers and procurement teams. Companies are drawn from official medicine registers and industry directories, with each one's own website where one is on file, so a search returns the makers themselves: verified website, sourcing contact, the markets where they are registered and, where published, the registered price.

Search by molecule or brandType an INN, an API or a brand name and see who makes it, in which country and dosage form.
Reach the maker directlyCompany email, website and address from the manufacturer's own site, never a trader's.
Regulatory standing in one placeGMP and inspection records, national registrations, WHO prequalification.
Refreshed from official sourcesNational registries and manufacturer sites are re-read on a schedule, so what you see is current.

Plans from $20 a month, billed annually Create an account

What you can search for

API and bulk drug substance suppliersManufacturers of active pharmaceutical ingredients, with their US DMF filings and GMP records, for a second source or a new formulation.
Finished dosage form manufacturersMakers of tablets, capsules, injectables, syrups and other finished medicines, by molecule, brand and country, with the dosage forms they register.
Contract manufacturers (CDMO / CMO)Companies that make the finished dose for a brand owner, identified separately from brand owners so you approach the right party.
GMP-certified and inspected sitesEU, UK and Swiss GMP certificates, US FDA inspection outcomes and WHO prequalification, each traced to the register it comes from. Claims found only in industry directories are marked as such.
Drug registrations by countryWhich product is registered in which market, by whom and, where a registry publishes it, at what price: the import-opportunity view for distributors.
Reference standard suppliersOfficial European Pharmacopoeia (EDQM) reference standards, listed by molecule beside the API and finished-dose makers.

Built for pharmaceutical importers and distributors, procurement and sourcing teams, business development, regulatory affairs and tender teams. Manufacturers from India, China, Turkey, Egypt, Jordan, the European Union, the United Kingdom, the United States, Latin America and South-East Asia; registrations from national medicine registries in 56 markets.

Questions buyers ask

What is PharmaOneLink?

PharmaOneLink is a searchable directory of verified pharmaceutical manufacturers for buyers, importers, distributors and procurement teams. It covers API (bulk drug substance) suppliers, finished dosage form makers, contract manufacturers (CDMO/CMO) and official reference standard suppliers, with each company's own website and sourcing contact.

How do I find who manufactures a molecule?

Type the molecule (INN or API name, e.g. atorvastatin, metformin, amoxicillin) or a brand name. Brand names are resolved to the active ingredient, so a search for Lipitor shows the makers of atorvastatin. The results list the manufacturers on file for that molecule, strongest evidence first, by country, with dosage forms, certifications and contact routes.

Does it cover API suppliers as well as finished-dose manufacturers?

Yes. Each company card states what it offers for the searched molecule: bulk API, finished dosage forms (tablets, capsules, injectables and so on), or an official pharmacopoeial reference standard. You can filter to API only, finished only or reference standards.

How are manufacturers verified?

Most companies are matched to an official regulatory record: a national medicines registration, a GMP certificate or inspection outcome (EU, UK, Swiss, US FDA), a US Drug Master File (DMF), an EDQM Certificate of Suitability (CEP) or WHO prequalification. The rest come from industry directories. Websites are identity-checked so that namesakes, traders and brokers are removed. Each profile shows the evidence behind every badge, and which ones rest on a directory listing only.

Which countries and markets are covered?

Manufacturers are based in more than 100 countries, including India, China, Turkey, Egypt, Jordan, the European Union, the United Kingdom, the United States, Latin America and South-East Asia. The registration layer reads national medicine registries in 56 markets across the Middle East, Africa, Europe, the Americas and Asia, so you can see where a product is already registered and who holds it.

What contact details do I get?

The manufacturer's own sales or export email, phone number, enquiry form and website, taken from the company's site, never a trader's listing. Where a national registry publishes the registered price, that is shown too.

Can I see where a product is already registered and who distributes it?

Yes. For each molecule or brand the registration panel lists the countries where it is registered, how many companies hold it there and their names, so you can tell whether a market is open or taken before you approach a maker.

Who uses PharmaOneLink?

Pharmaceutical importers and distributors looking for products to register, procurement and sourcing teams looking for a second API source, business development teams searching for partners in a new market, regulatory affairs staff checking registrations, and tender participants who need a manufacturer's direct contact.

What does it cost?

One plan with the whole directory: 60 US dollars a month, 150 dollars a quarter or 240 dollars a year (20 dollars a month). Billing is handled by Paddle; cancel from your account at any time.

Is the data available through an API, bulk export or scraping?

No. Profiles may be used and exported for your own sourcing work. Automated access, crawling, bulk extraction or redistribution of the directory is prohibited by the Terms and is pursued. Team licences are available on request.