Guerbet
Formulazioni farmaceutiche, medicinali generici e prodotti sanitari.
Guerbet produce formulazioni farmaceutiche, medicinali generici e prodotti sanitari dalle sue attività a Villepinte. L'azienda fornisce canali farmaceutici, acquirenti ospedalieri, distributori sanitari o clienti esportatori nei mercati primari elencati.
- Type
- brand seeking distribution
- Location
- Villepinte, France
- Founded
- 1926
- Website
- guerbet.com
- Categories
- Forniture medicali e sanitarie, Integratori e benessere
- Markets
- Francia, Stati Uniti, Germania, Giappone
Verified facts
- operating-permit (green), checked 2026-08-04 Georisques, French register of classified installations (ICPE)
- facility-inspected (green), checked 2026-08-20 Georisques, French register of classified installations (ICPE)
- workforce-on-record (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- aeo-certified (green), checked 2026-08-30 EU AEO register (European Commission)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- domain-registered (green), checked 2026-08-26 Domain registry record
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-08-30 Registre national des producteurs (ADEME/SYDEREP), France
- registry-active-global (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), 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
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- registry-activity (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- facility-registered (green), checked 2026-08-30 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- industrial-site-registered (green), checked 2024-12-31 IREP, French register of pollutant releases and waste (declared by the operator)
- media-mention (green), checked 2026-07-18 Radiology Business
- gmp-certified (green), checked 2024-04-26 EudraGMDP, EU register of GMP certificates (EMA)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- AEO, Authorised Economic Operator EU AEO database
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)