Ipsen
药物制剂、仿制药和保健品。
益普生 (Ipsen) 在巴黎的工厂生产药物制剂、仿制药和保健品。该公司向其上市主要市场的药房渠道、医院买家、医疗保健分销商或出口客户提供服务。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Paris, France
- Founded
- 1929
- Website
- ipsen.com
- Categories
- 医疗保健用品, 补充剂与健康
- Markets
- 法国, 美国, 德国, 日本
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)