Ali Bin Ali Holding
Katarska główna sieć dystrybucji importowanego sprzętu konsumenckiego i sprzętu medycznego
Ali Bin Ali Holding zarządza kompleksowymi strukturami dostaw aktywów farmaceutycznych i dóbr luksusowych światowych marek spożywczych. Ich centra realizacji zapewniają pełną obsługę korporacyjnych sieci detalicznych i opieki zdrowotnej.
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Doha, Qatar
- Founded
- 1945
- Website
- alibinali.com
- Categories
- Spiżarnia i towary suche, Opieka osobista, Artykuły medyczne i związane z opieką zdrowotną
- Markets
- Katar, Arabia Saudyjska
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 2026-08-04 Mail server of the company domain
- domain-registered (green), checked 2026-08-04 Domain registry record
- sanctions-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-04 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 22000, Food Safety IAF CertSearch
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)