VERDOT
Downstream Purification Equipment | VERDOT
Verdot, opgericht in 1950 en met hoofdkantoor in Riom, Frankrijk, loopt voorop op het gebied van downstream bioprocessingtechnologie. Verdot richt zich op innovatieve zuiveringsoplossingen voor de…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://verdot-biotechnologies.com
- Categories
- Farmaceutische productie
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
- 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)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- facility-registered (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-active-global (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- registry-activity (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- domain-registered (green), checked 2026-08-26 Domain registry record
- listed-in-registry (amber), checked 2026-08-26 BRIS, EU business registers interconnection (e-justice.europa.eu)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
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)