Grunenthal
Farmasötik formülasyonlar, jenerik ilaçlar ve sağlık ürünleri.
Grunenthal, Aachen operasyonlarından farmasötik formülasyonlar, jenerik ilaçlar ve sağlık ürünleri üretmektedir. Şirket, listelenen birincil pazarlarda eczane kanallarına, hastane alıcılarına, sağlık distribütörlerine veya ihracat müşterilerine hizmet vermektedir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Aachen, Germany
- Founded
- 1946
- Website
- grunenthal.com
- Categories
- Tıbbi ve Sağlık Malzemeleri, Takviyeler ve Sağlık
- Markets
- Almanya, Amerika Birleşik Devletleri, Fransa, İspanya
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
- 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 2026-09-07 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, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
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)