Guerbet
Formulations pharmaceutiques, médicaments génériques et produits de santé.
Guerbet fabrique des formulations pharmaceutiques, des médicaments génériques et des produits de santé depuis ses activités de Villepinte. La société approvisionne les réseaux de pharmacies, les acheteurs d'hôpitaux, les distributeurs de soins de santé ou les clients exportateurs sur ses principaux marchés cotés.
- Type
- Manufacturer
- Location
- Villepinte, France
- Founded
- 1926
- Website
- guerbet.com
- Categories
- Fournitures médicales et de santé, Compléments et bien-être
- Markets
- France, États-Unis, Allemagne, Japon
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)
- domain-registered (green), checked 2026-07-28 Domain registry record
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-08-16 Registre national des producteurs (ADEME/SYDEREP), France
- registry-active-global (green), checked 2026-08-19 INSEE Sirene (annuaire-entreprises)
- facility-registered (green), checked 2026-08-16 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- 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
- industrial-site-registered (green), checked 2024-12-31 IREP, French register of pollutant releases and waste (declared by the operator)
- aeo-certified (green), checked 2026-08-16 EU AEO register (European Commission)
- 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)