Emzor Pharmaceutical Industries Limited
Emzolyn, Emtrix 및 광범위한 필수 의약품 포트폴리오를 갖춘 나이지리아 제약 제조업체입니다.
Emzor Pharmaceutical Industries Limited는 나이지리아 의료 시장을 위한 정제, 시럽, 연고 및 주사제를 제조합니다. 해당 제품에는 기침 시럽, 진통제, 항말라리아제, 영양 보충제가 포함됩니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Isolo, Nigeria
- Founded
- 1984
- Website
- https://www.emzorpharma.com
- Categories
- 보충제 및 웰니스, 의료 및 건강 관리 용품
- Markets
- 나이지리아, 가나, 코트디부아르
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
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-08 - 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 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- web-presence-since (green), checked 2026-08-02 Internet Archive (Wayback)
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- 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)