Delpharm
Delpharm is een wereldleider op het gebied van farmaceutische ontwikkeling en productie en behoort tot de top vijf van CDMO's wereldwijd
Delpharm is een wereldleider op het gebied van farmaceutische ontwikkeling en productie en behoort tot de top vijf van CDMO's wereldwijd. Het bedrijf is gespecialiseerd in de ontwikkeling van geneesmiddelen, ondersteuning op het gebied van regelgeving,…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://delpharm.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
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- 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)
- 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)
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- 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
- domain-registered (green), checked 2026-08-26 Domain registry record
- media-mention (green), checked 2026-07-18 Contract Pharma
- 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)