Where EFDA publishes registrations
EFDA runs eRIS, its online regulatory information system. Its public pages let anyone look up registered products and the manufacturers behind them; older registrations were also published as lists on EFDA's website.
- 1
Open eRIS
Go to EFDA's eRIS portal and open the public product or manufacturer listing.
- 2
Search by name
Search by generic name, brand name or manufacturer. Try spelling variants and salt forms: registrations follow the dossier's wording.
- 3
Read the status
Check that the registration is current, for the right strength, dosage form or device model, and for the manufacturing site you ship from.
What the result means
- Registered and current: importers can apply for an import permit for each shipment.
- Registered, but not your site, strength or model: that variant needs its own registration or a variation.
- Not registered: it needs EFDA registration through a local agent first; special import permits exist only for shortages and emergencies, case by case.
Then: who already imports it?
Registration tells you whether a product may be imported; HealthTrade Data shows how often it actually is, by how many Ethiopian companies and from which countries. Search the product on our market pages, and if it isn't registered yet, we can register it for you.
Frequently asked questions
Is there an official EFDA registered products list?+
Yes. EFDA publishes registered products and manufacturers through its eRIS portal; search there by generic name, brand or manufacturer.
Where can I find EFDA registered suppliers?+
eRIS lists the manufacturers whose products are registered. To see which Ethiopian companies import a product, and from which suppliers, use HealthTrade Data's market pages.
What if my product is not registered in Ethiopia?+
It has to be registered with EFDA through a licensed local agent before importers can bring it in routinely. HealthTrade Data offers registration of medicines and medical devices through a licensed local agent.
Official sources
- EFDA eRIS portal
- EFDA: Guideline for Registration of Medicine (2024)
- EFDA: Guidelines for registration of medical devices and supplies
- EFDA: Guideline on medical products special import permit (2023)
This guide is general information, not legal or regulatory advice. Always check EFDA's current guideline before you submit.