Biopharma Technologies France
法国制药制造
Biopharma Technologies France 是一家总部位于法国的制药公司。
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- France
- Website
- https://biopharmatech.fr
- Categories
- 药品制造
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)
- registered-trade-only (amber), 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
- domain-registered (green), checked 2026-08-26 Domain registry record
- financials-published (green), effective since 2019-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- public-contract-awarded (green), effective since 2026-07-22 DECP, French public-procurement register 在这里，中标还附带了别人做过的审查：在欧盟和欧洲经济区，公共采购方必须排除因欺诈、腐败或洗钱被定罪的投标人，以及经终局裁决认定拖欠税款或社会保险费的投标人。 Directive 2014/24/EU, Article 57 (exclusion grounds)
- registry-id-verified (green), checked 2026-08-20 SIREN published in the company's own legal notice, confirmed in the French business register
- registry-active-global (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
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)