LABORATOIRES URGO (URGO MEDICAL - MDFA (MEDICAL DEVICE FOR ALL))
医薬品製造、フランス
LABORATOIRES URGO (URGO MEDICAL - MDFA (MEDICAL DEVICE FOR ALL)) は、フランスのシュノーヴに拠点を置く医薬品製造会社です。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Chenove, France
- Founded
- 2000
- Website
- http://www.urgo.fr
- Categories
- 医薬品製造
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
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
- domain-registered (green), checked 2026-07-28 Domain registry record
- facility-inspected (green), checked 2026-08-20 Georisques, French register of classified installations (ICPE)
- workforce-on-record (green), effective since 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- places-goods-on-market (green), checked 2026-09-07 Registre national des producteurs (ADEME/SYDEREP), France
- public-contract-awarded (green), effective since 2026-06-26 TED (Tenders Electronic Daily), EU public procurement award notices ここでの落札は、他者による審査も伴います。EUおよびEEAでは、公共調達者は詐欺、汚職、資金洗浄で有罪となった入札者、および確定した決定で税や社会保険料の未納が認定された入札者を排除しなければなりません。 Directive 2014/24/EU, Article 57 (exclusion grounds)
- financials-published (green), effective since 2019-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- registry-activity (green), checked 2026-09-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- industrial-site-registered (green), effective since 2024-12-31 IREP, French register of pollutant releases and waste (declared by the operator)
- facility-activity-described (green), checked 2026-08-20 Georisques, French register of classified installations (ICPE)
- operating-permit (green), effective since 2026-04-28 Georisques, French register of classified installations (ICPE)
- registered-manufacturer (green), checked 2026-09-17 Ministero della Salute, banca dati e Repertorio dei dispositivi medici
- directors-on-file (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- registry-active-global (green), checked 2026-09-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- registered-address (green), checked 2026-08-10 INSEE Sirene (annuaire-entreprises)
- vat-valid (green), checked 2026-08-05 VIES (European Commission)
- export-registered (green), checked 2026-09-21 EU EORI validation (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)