VERDOT
Downstream Purification Equipment | VERDOT
Verdot, được thành lập vào năm 1950 và có trụ sở chính tại Riom, Pháp, đi đầu trong công nghệ xử lý sinh học hạ nguồn. Verdot tập trung vào các giải pháp thanh lọc tiên tiến cho…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://verdot-biotechnologies.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
- 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)