VENIPHARM
Venipharm
Venipharm, jenerik ilaç pazarlama izin başvurularının geliştirilmesi ve tescili konusunda uzmanlaşmış bağımsız bir ilaç şirketidir. Paris ve Hamburg'da ofisleri bulunan…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://venipharm.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)
- registered-since (green), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- domain-registered (green), checked 2026-08-26 Domain registry record
- places-goods-on-market (green), checked 2026-09-07 Registre national des producteurs (ADEME/SYDEREP), France
- registry-active-global (green), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- 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
- 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
- registered-trade-only (amber), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-08-26 INSEE Sirene (annuaire-entreprises)
- gmp-certified (green), effective since 2023-04-05 EudraGMDP, EU register of GMP certificates (EMA)
- 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)