Biotrial
풀 서비스 CRO | 임상 연구 서비스 | 생체시험
Biotrial은 생명공학 제약회사를 대상으로 전임상 및 임상 연구를 수행하는 의약품 개발 전문 CRO입니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- France
- Website
- https://biotrial.com
- Categories
- 의약품 제조
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)