Dechra Pharmaceuticals
Formulaciones farmacéuticas, medicamentos genéricos y productos sanitarios.
Dechra Pharmaceuticals fabrica formulaciones farmacéuticas, medicamentos genéricos y productos sanitarios en sus operaciones de Northwich. La empresa abastece a canales de farmacias, compradores de hospitales, distribuidores de atención médica o clientes de exportación en sus mercados primarios listados.
- Type
- brand seeking distribution
- Location
- Northwich, United Kingdom
- Founded
- 1997
- Website
- dechra.com
- Categories
- Suministros médicos y sanitarios, Suplementos y bienestar
- Markets
- Reino Unido, Estados Unidos, Alemania, Francia
Verified facts
- officer-appointed (green), checked 2026-08-28 Companies House (officers)
- leadership-on-record (green), checked 2026-08-28 Companies House (officers)
- ownership-on-record (green), checked 2026-08-28 Companies House (PSC)
- annual-accounts-filed (green), checked 2026-08-28 Companies House (accounts)
- domain-registered (green), checked 2026-08-28 Domain registry record
- sanctions-clear (green), checked 2026-08-28 OpenSanctions
- debarment-clear (green), checked 2026-08-28 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-28 Mail server of the company domain
- directors-on-file (green), checked 2026-08-28 Companies House
- licensed-sponsor (green), checked 2026-08-12 UK Home Office register of licensed sponsors (workers)
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- registered-since (green), checked 1997-05-13 Companies House free company data product (UK)
- ch-active (green), checked 2026-08-28 Companies House
- media-mention (green), checked 2026-07-18 GOV.UK
Claimed certifications
- 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)