ACDIMA International
Empresa pan-árabe de aparelhos farmacêuticos e médicos fundada em 1976 pelo Conselho de Unidade Econômica Árabe.
ACDIMA (Empresa Árabe para Indústrias Farmacêuticas e Aparelhos Médicos) foi criada em 6 de março de 1976 por resolução do Conselho de Unidade Econômica Árabe com capital inicial de 60 milhões de dinares do Kuwait. A empresa comercializa produtos farmacêuticos e de suas subsidiárias no mundo árabe. Seu CRO de bioequivalência afiliado, ACDIMA Center, está sediado em Amã.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Amman, Jordan
- Founded
- 1976
- Website
- acdima.com
- Categories
- Suprimentos médicos e de saúde
- Markets
- Emirados Árabes Unidos, Arábia Saudita, Egito, Alemanha, Reino Unido
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)