Kuwait Saudi Pharmaceutical Industries Co.
クウェート・サウジ・ファーマシューティカル・インダストリーズ社、輸出対応のB2Bチャネル向けジェネリック医薬品を製造
クウェート・サウジ・ファーマシューティカル・インダストリーズ社は、クウェート市でジェネリック医薬品、医薬品製剤、ヘルスケア製品を製造しています。 1980 年に設立された同社は、KW、SA、AE、QA および関連輸出市場にわたる薬局、病院、公共入札、販売代理店に製品を供給しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Kuwait City, Kuwait
- Founded
- 1980
- Website
- kspico.com
- Categories
- 医療およびヘルスケア用品
- Markets
- クウェート, サウジアラビア, アラブ首長国連邦, カタール
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
- domain-registered (green), checked 2026-08-09 Domain registry record
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registered-manufacturer (green), checked 2026-08-30 Public Authority for Industry, Kuwait (industrial directory)
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)