LFB Biomanufacturing
LFB Biomanufacturing là tổ chức sản xuất và phát triển theo hợp đồng (CDMO) chuyên sản xuất protein tái tổ hợp và kháng thể đơn dòng cho
LFB Biomanufacturing là tổ chức sản xuất và phát triển theo hợp đồng (CDMO) chuyên sản xuất protein tái tổ hợp và kháng thể đơn dòng cho ngành công nghiệp dược phẩm sinh học. Cái…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://lfb.fr
- Categories
- Sản xuất dược phẩm
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)