Biotrial
CRO đầy đủ dịch vụ | Dịch vụ nghiên cứu lâm sàng | Thử nghiệm sinh học
Biotrial là CRO chuyên phát triển thuốc thực hiện các nghiên cứu tiền lâm sàng và lâm sàng cho các công ty dược phẩm công nghệ sinh học.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- https://biotrial.com
- Categories
- Sản xuất dược phẩm
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)
- 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)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- 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)
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- directors-on-file (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- domain-registered (green), checked 2026-08-26 Domain registry record
- media-mention (green), checked 2026-07-18 Reuters
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- 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)