Ipsen
Farmasötik formülasyonlar, jenerik ilaçlar ve sağlık ürünleri.
Ipsen, Paris 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
- Paris, France
- Founded
- 1929
- Website
- ipsen.com
- Categories
- Tıbbi ve Sağlık Malzemeleri, Takviyeler ve Sağlık
- Markets
- Fransa, Amerika Birleşik Devletleri, Almanya, Japonya
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
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- workforce-on-record (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- domain-registered (green), checked 2026-08-26 Domain registry record
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registry-active-global (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- 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)