LFB Biomanufacturing
LFB Biomanufacturing は、バイオ医薬品産業向けの組換えタンパク質とモノクローナル抗体の生産を専門とする受託開発製造組織 (CDMO) です。 …
LFB Biomanufacturing は、バイオ医薬品産業向けの組換えタンパク質とモノクローナル抗体の生産を専門とする受託開発製造組織 (CDMO) です。 …
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://lfb.fr
- Categories
- 医薬品製造
Listed in a source registry
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)
- registered-since (green), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- domain-registered (green), checked 2026-08-26 Domain registry record
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- debarment-clear (green), checked 2026-08-26 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- registry-active-global (green), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- facility-registered (green), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- sanctions-clear (green), checked 2026-08-26 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registry-activity (green), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- media-mention (green), checked 2026-07-18 Contract Pharma
- gmp-certified (green), effective since 2025-11-07 EudraGMDP, EU register of GMP certificates (EMA)
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)