Grunenthal
Фармацевтические составы, дженерики и товары медицинского назначения.
Grunenthal производит фармацевтические препараты, дженерики и товары медицинского назначения на своих предприятиях в Ахене. Компания поставляет продукцию аптекам, покупателям больниц, дистрибьюторам медицинских услуг или экспортным клиентам на перечисленных основных рынках.
- Type
- brand seeking distribution
- Location
- Aachen, Germany
- Founded
- 1946
- Website
- grunenthal.com
- Categories
- Медицинские товары и расходники, БАДы и товары для здоровья
- Markets
- Германия, Соединенные Штаты, Франция, Испания
Verified facts
- domain-registered (green), checked 2026-08-02 Domain registry record
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
Profiles
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- AEO, Authorised Economic Operator EU AEO database
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- 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)