Addis Pharmaceutical Factory
埃塞俄比亚私营制药商提供价格实惠的仿制药。
亚的斯制药厂为埃塞俄比亚医疗保健市场生产口服固体剂型、液体和半固体剂型。它通过公共采购和私人药房连锁店进行分销。
- 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
- 医疗保健用品
- Markets
- 埃塞俄比亚
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)