ACDIMA International
アラブ経済統一評議会によって 1976 年に設立された汎アラブの製薬および医療機器会社。
ACDIMA (医薬品産業および医療機器のためのアラブ会社) は、アラブ経済統一評議会の決議により 1976 年 3 月 6 日に設立され、当初資本金は 6,000 万クウェート ディナールでした。同社はアラブ世界内で医薬品およびその子会社の医薬品を販売しています。その関連生物同等性 CRO、ACDIMA センターはアンマンに拠点を置いています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Amman, Jordan
- Founded
- 1976
- Website
- acdima.com
- Categories
- 医療およびヘルスケア用品
- Markets
- アラブ首長国連邦, サウジアラビア, エジプト, ドイツ, イギリス
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
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- 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
- 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
- domain-registered (green), checked 2026-08-03 Domain registry record
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
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)