CIPHARM
제네릭 의약품, 정제, 시럽 및 의약품 제제.
CIPHARM은 Abidjan 사업장에서 제네릭 의약품, 정제, 시럽 및 의약품 제제를 제조합니다. 이 회사는 나열된 주요 시장 전반에 걸쳐 약국 채널, 병원 구매자, 의료 유통업체 또는 수출 고객에게 제품을 공급합니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Abidjan, Côte d'Ivoire
- Founded
- 1988
- Website
- cipharm.ci
- Categories
- 의료 및 건강 관리 용품, 보충제 및 웰니스
- Markets
- 코트디부아르, 세네갈, 가나, 카메룬
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
- debarment-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-05 - 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 2026-08-05 Mail server of the company domain
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)