AstraZeneca PLC
Công ty dược phẩm sinh học toàn cầu phát triển và sản xuất thuốc điều trị ung thư, tim mạch và hô hấp…
Công ty dược phẩm sinh học toàn cầu phát triển và sản xuất các sản phẩm thuốc điều trị ung thư, tim mạch và hô hấp.
- Type
- brand seeking distribution
- Location
- Cambridge, United Kingdom
- Founded
- 1999
- Website
- astrazeneca.com
- Categories
- Vật tư y tế và chăm sóc sức khỏe
- Markets
- Hoa Kỳ, Trung Quốc, Nhật Bản, Đức, Vương quốc Anh
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), checked 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), checked 1992-06-17 Companies House free company data product (UK)
- registered-trade-role (green), checked 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
Claimed certifications
- 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)