Addis Pharmaceutical Factory
شركة تصنيع أدوية إثيوبية خاصة توفر أدوية عامة بأسعار معقولة.
يقوم مصنع أديس للأدوية بتصنيع أشكال الجرعات الصلبة عن طريق الفم والسوائل والمواد شبه الصلبة لسوق الرعاية الصحية الإثيوبي. يتم توزيعها من خلال المشتريات العامة وسلاسل الصيدليات الخاصة.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Addis Ababa, Ethiopia
- Founded
- 1998
- Website
- https://www.addispharma.com
- Categories
- اللوازم الطبية والرعاية الصحية
- Markets
- إثيوبيا
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
- domain-registered (green), checked 2026-08-03 Domain registry record
- debarment-clear (green), checked 2026-08-03 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-03 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- listed-in-registry (green), checked 2026-08-21 FDRE Ministry of Education, Higher Education, TVET & Research Industry Innovation Linkage System (HETRIIL) industry profiles
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)