AstraZeneca PLC
Perusahaan biofarmasi global yang mengembangkan dan memproduksi onkologi, kardiovaskular, dan pernapasan…
Perusahaan biofarmasi global yang mengembangkan dan memproduksi produk obat onkologi, kardiovaskular, dan pernapasan.
- 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
- Perlengkapan Medis & Kesehatan
- Markets
- Amerika Serikat, Tiongkok, Jepang, Jerman, Inggris Raya
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)