SKYEPHARMA
Discover a French independent CDMO specialist in complex projects and highly potent APIs
Skyepharma là Tổ chức Sản xuất và Phát triển Hợp đồng (CDMO) tích hợp đầy đủ chuyên về các dạng bào chế uống phức tạp, cung cấp một loạt các dịch vụ toàn diện từ phát triển…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- http://skyepharma.fr
- 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)
- facility-registered (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- registry-activity (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- registry-active-global (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- registered-trade-only (amber), 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
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- domain-registered (green), checked 2026-08-26 Domain registry record
- media-mention (green), checked 2026-07-18 BioSpace
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
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)