Cebiphar SA
Cebiphar offers its expertise to the Health industries
Cebiphar SA, ilaç endüstrisinin saygın bir tedarikçisidir ve düzenleyici kurumların karmaşık ihtiyaçlarını desteklemeyi amaçlayan bir dizi hizmet sağlamada uzmanlaşmıştır…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Founded
- 1979
- Website
- http://cebiphar.com
- Categories
- İlaç Üretimi
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)
- 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)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- domain-registered (green), checked 2026-08-26 Domain registry record
- registry-active-global (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- directors-on-file (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- registry-id-verified (green), checked 2026-08-20 SIREN published in the company's own legal notice, confirmed in the French business register
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- listed-in-registry (amber), checked 2026-08-26 BRIS, EU business registers interconnection (e-justice.europa.eu)
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)