Guerbet
Pharmazeutische Formulierungen, Generika und Gesundheitsprodukte.
Guerbet stellt in seinem Werk in Villepinte pharmazeutische Formulierungen, Generika und Gesundheitsprodukte her. Das Unternehmen beliefert Apothekenkanäle, Krankenhauseinkäufer, Vertriebshändler im Gesundheitswesen oder Exportkunden in seinen aufgeführten Hauptmärkten.
- Type
- brand seeking distribution
- Location
- Villepinte, France
- Founded
- 1926
- Website
- guerbet.com
- Categories
- Medizin- & Gesundheitsbedarf, Nahrungsergänzung & Wellness
- Markets
- Frankreich, Vereinigte Staaten, Deutschland, Japan
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)