AstraZeneca PLC
종양학, 심혈관, 호흡기 분야를 개발 및 제조하는 글로벌 바이오제약 기업
종양학, 심혈관, 호흡기 관련 의약품을 개발 및 제조하는 글로벌 바이오제약 기업입니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Cambridge, United Kingdom
- Founded
- 1999
- Website
- astrazeneca.com
- Categories
- 의료 및 건강 관리 용품
- Markets
- 미국, 중국, 일본, 독일, 영국
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
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- product-authorised-for-sale (green), checked 2026-08-21 Gobiernu di Korsou, Lijst maximumprijzen geneesmiddelen (bijlage bij de Regeling maximumprijzen geneesmiddelen)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- industrial-permit (green), checked 2026-08-11 Environment Agency public register, environmental permits (England)
- domain-registered (green), checked 2026-08-28 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-28 Mail server of the company domain
- registry-active-global (green), checked 2026-08-24 Environment Agency public registers (England)
- registry-activity (green), effective since 1992-06-17 Companies House free company data product (UK)
- debarment-clear (green), checked 2026-08-28 OpenSanctions
- sanctions-clear (green), checked 2026-08-28 OpenSanctions
- operating-permit (green), checked 2026-08-12 MHRA register of licensed manufacturing and wholesale dealer sites (UK)
- licensed-sponsor (green), checked 2026-08-12 UK Home Office register of licensed sponsors (workers)
- registered-since (green), effective since 1992-06-17 Companies House free company data product (UK)
- registered-trade-role (green), effective since 2026-08-01 Companies House free company data product (UK)
- directors-on-file (green), checked 2026-06-20 Companies House
- ch-active (green), checked 2026-06-20 Companies House
- media-mention (green), checked 2026-07-18 Yahoo Finance
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- FDA Registered FDA Establishment Registration
- ISO 13485, Medical Devices Quality 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)