Confirm the exact product, intended use, manufacturer and device class where relevant.
Responsible imports
start with readiness.
Pharmaceutical and medical device imports are subject to product-specific regulatory and documentation requirements.
OUR APPROACH
Verify the details
for each product.
Safe Life treats import readiness as a product-by-product responsibility.
Requirements may differ by product type and device class. Before import or supply, Safe Life confirms the applicable importer authorizations, market registrations or special permissions, permits and clearance documents against current Ethiopian Food and Drug Authority requirements.
Check the permissions and product authorization that apply to the item and transaction.
Confirm import permits and the documents required for clearance before shipment.
EFDA publishes separate guidance for medicine imports, registration and medical device clearance. Requirements can change; confirm the current rules with the relevant authority before proceeding.
Ethiopian Food and Drug Authority ↗