VENIPHARM
Venipharm
Venipharm là một công ty dược phẩm độc lập chuyên phát triển và đăng ký các ứng dụng cấp phép lưu hành thuốc generic. Với văn phòng đặt tại Paris và Hamburg,…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://venipharm.com
- 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)
- 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)