Dechra Pharmaceuticals
Фармацевтические составы, дженерики и товары медицинского назначения.
Dechra Pharmaceuticals производит фармацевтические препараты, непатентованные лекарства и товары медицинского назначения на своих предприятиях в Нортвиче. Компания поставляет продукцию аптекам, покупателям больниц, дистрибьюторам медицинских услуг или экспортным клиентам на перечисленных основных рынках.
- Type
- brand seeking distribution
- Location
- Northwich, United Kingdom
- Founded
- 1997
- Website
- dechra.com
- Categories
- Медицинские товары и расходники, БАДы и товары для здоровья
- Markets
- Великобритания, Соединенные Штаты, Германия, Франция
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)