We work with international and local manufacturers and suppliers of medicines, medical supplies, medical equipment, and laboratory reagents that meet EFDA and WHO-GMP requirements. Each partnership is evaluated on a product-by-product basis.
Yes.
In Ethiopia, each shipment requires EFDA import authorization and release approval. Products are distributed only after EFDA inspection and clearance of the specific consignment.
Required documents may include:
Specific requirements may vary by product category.
The timeline depends on:
Completeness of documentation
EFDA registration requirements
Product category and regulatory pathway
Initial document review typically takes 1–2 weeks, while EFDA registration and shipment approvals follow regulatory timelines.
Yeteref Bet Pharmaceuticals manages EFDA coordination, import permit applications, and regulatory follow-ups, in close collaboration with the manufacturer or supplier.
We distribute to hospitals, clinics, pharmacies, wholesalers, NGOs, and public health programs across multiple regions in Ethiopia.
Yes.
Where applicable, we share sales trends, regulatory updates, and market feedback to support planning and compliance.
You can submit a Partnership Inquiry through our website or contact our business development team directly. Our team will review your submission and respond within 24–48 business hours.