Pharmaceutical supply to Yemen, for aid programmes and licensed importers

Yes. Progene Pharma manufactures generic medicines in a WHO-GMP certified facility and supplies them to importers, wholesalers, hospital suppliers and tender suppliers in Yemen.

Yes. Progene Pharma prepares the documents the Supreme Board registration needs: a CTD dossier with Zone IVb stability data, the WHO-format COPP, the GMP certificate, the letter of authorisation and samples for testing. Your Yemeni company submits the application, and we answer the Supreme Board's questions with you.

For commercial supply, yes: a medicine is registered through a licensed Yemeni importer with the relevant authority for its area. A programme buyer follows its own rules instead. Check the current requirements with the authority and your buyer.

It varies by product and by how complete the dossier is, from several months to more than a year. A complete dossier with clear stability data and prompt answers to the Supreme Board's questions helps. Many importers register a few products first and add more as orders grow.

The usual set is a CTD dossier, a COPP, a GMP certificate, stability data, a letter of authorisation, product samples and artwork. the Supreme Board updates its requirements from time to time, so confirm the current list with the Supreme Board or your regulatory agent. We tell you what we can provide with your quotation.

Yes. We supply programme and hospital packs with the full document set that international organisations expect, including the COPP, GMP certificate and COA. Send us the programme's specification and we will confirm what we can provide.

Conditions at the ports, with banks and on the roads change quickly. We confirm routes, permits and payment arrangements with the buyer before we accept an order, and we plan each shipment individually.

The Supreme Board of Drugs and Medical Appliances is the main regulator, but the country has more than one administration and each may set its own requirements. Check the current rules for the area you supply with your importer or your programme's procurement team.

English text, with Arabic where the buyer or the authority asks for it, the registration number where required, batch number, manufacture and expiry dates, storage conditions and the other details the buyer requires. We prepare the artwork and you approve a proof before printing.

Yes. Products for this market are tested at 30 °C and 75% relative humidity (Zone IVb) and packed in moisture-resistant blisters or bottles, so the shelf life stays valid in hot, humid conditions.

Yes. Progene Pharma supplies tender packs and the product documents tenders usually ask for, such as the COPP, GMP certificate and COA. Tell us the tender requirements and we will confirm what we can provide.

Progene Pharma ships by sea from Nhava Sheva (JNPT) near Mumbai to Aden, or through Djibouti for onward transport, on FOB, CFR or CIF terms. Routes and schedules change with conditions, so we confirm them with your quotation.

It depends on the product, the dosage form and the packaging. We work with large importers and tender suppliers as well as smaller distributors, and confirm the minimum quantity with your quotation.