Diverchim CDMO
DIVERCHIM CDMO
Diverchim là CDMO hàng đầu của Pháp chuyên về hóa học phức tạp và sản xuất API quy mô nhỏ. Được thành lập với mục tiêu tập trung vào phát triển dược chất, Diverchim vượt trội trong…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://diverchim.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)
- certificate-page-on-site (amber), checked 2026-09-18 Company's own certification page
- 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)
- facility-registered (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- 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)
- registry-id-verified (green), checked 2026-08-20 SIREN published in the company's own legal notice, confirmed in the French business register
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- domain-registered (green), checked 2026-08-26 Domain registry record
- gmp-certified (green), effective since 2022-06-16 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)