Dechra Pharmaceuticals
Pharmazeutische Formulierungen, Generika und Gesundheitsprodukte.
Dechra Pharmaceuticals stellt in seinem Betrieb in Northwich pharmazeutische Formulierungen, Generika und Gesundheitsprodukte her. Das Unternehmen beliefert Apothekenkanäle, Krankenhauseinkäufer, Vertriebshändler im Gesundheitswesen oder Exportkunden in seinen aufgeführten Hauptmärkten.
- Type
- brand seeking distribution
- Location
- Northwich, United Kingdom
- Founded
- 1997
- Website
- dechra.com
- Categories
- Medizin- & Gesundheitsbedarf, Nahrungsergänzung & Wellness
- Markets
- Vereinigtes Königreich, Vereinigte Staaten, Deutschland, Frankreich
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)