Global B2B Pharmaceutical Sourcing · Dossier Licensing · Named-Patient Access
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List your products, dossiers and partnership needs

For pharmaceutical manufacturers anywhere. Export finished products and APIs, out-license dossiers, find distributors, or fill contract-manufacturing capacity. List once, and we match you against live importer requirements.

List your assets
Mitul Agarwal
Written by Mitul Agarwal · B.Pharm, MBA
Founder & Head of Business Development · 25+ years in international pharmaceutical BD&L

What you can list

Export products

Finished formulations with your GMP approvals, CoPP availability and the countries you already supply.

APIs & intermediates

Active ingredients with CEP / DMF status for importers and local manufacturers.

Dossiers to license

CTD / ACTD dossiers and registered brands available for out-licensing, with BE status.

Distributors wanted

Tell us the countries where you want an importer or distribution partner.

CMO capacity

Spare capacity and dosage forms for brand owners and white-label buyers.

How it works

1

List once, no documents

A short form: what you want to do, your GMP approvals, dossier position and products. Upload your product list if it's easier.

2

We match you to live demand

Importers send us product lists and tenders. We match them to manufacturers whose approvals and dossiers fit the destination country.

3

You hear from us with a real requirement

Product, market and volume first. Dossier documents only once the requirement is firm, and only under a mutual CDA.

See what importers are asking for right now.
Live enquiries and the monthly Demand Index, updated from real RFQs.

Your dossier and your buyers stay protected

  • No documents to join. We ask only what you hold: approvals, dossier formats, BE position and products.
  • Documents only against a real requirement, and only after a signed mutual CDA that binds both sides.
  • Never circulated. Your documents are not shared with other manufacturers or used to pressure a competing quote.
  • You choose how you appear. Publish anonymously, publish with your name, or stay private and be matched quietly.
  • You approve the counterparty before your dossier reaches any buyer.

Manufacturer partnership form

1 · Your company
2 · What do you want to do? *

Tick all that apply.

3 · GMP approvals held *

Tick every approval currently valid for the site you would supply from.

4 · Dossier position
5 · Your products and markets
How we treat this. Nothing here is confidential and we are not asking for documents at this stage. We use it to match you to importer requirements, and we publish your listing only in the way you chose above.

Would rather talk before filling anything in?

Terms are often easier to settle in a conversation than on a form.

Arrange a call

Frequently asked questions

No. The first stage is a written statement of what you hold: GMP approvals, dossier formats, BE position and products. Documents are requested only when a specific buyer and requirement are on the table, and only under a signed mutual confidentiality agreement.

Only if you choose it. You can publish anonymously (country, approvals and products only), publish with your company name, or stay private and be matched without any public listing.

WHO-GMP is the practical baseline for most importing countries. EU-GMP, US FDA or PIC/S approval strengthens your position, especially for sterile products, biologics and regulated markets. Tell us what you hold and we will tell you where it is accepted.

List those countries under "already registered". We will not approach markets where you have an existing arrangement, and we will not contact your current partners.

Yes. Tick "Out-license dossiers or registered brands". Importers and local manufacturers that want their own registrations look for exactly that.

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