ACDIMA International
Pan-Arab ilaç ve tıbbi cihazlar şirketi, 1976 yılında Arap Ekonomik Birlik Konseyi tarafından kuruldu.
ACDIMA (Arap İlaç Endüstrisi ve Tıbbi Cihazlar Şirketi), 6 Mart 1976'da Arap Ekonomik Birlik Konseyi kararıyla 60 milyon Kuveyt Dinarı başlangıç sermayesiyle kuruldu. Şirket, farmasötik ürünleri ve yan kuruluşlarının ürünlerini Arap dünyasında pazarlamaktadır. Bağlı olduğu biyoeşdeğerlik CRO'su ACDIMA Merkezi'nin merkezi Amman'da bulunmaktadır.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Amman, Jordan
- Founded
- 1976
- Website
- acdima.com
- Categories
- Tıbbi ve Sağlık Malzemeleri
- Markets
- Birleşik Arap Emirlikleri, Suudi Arabistan, Mısır, Almanya, Birleşik Krallık
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)