Guerbet
फार्मास्युटिकल फॉर्मूलेशन, जेनेरिक दवाएं और स्वास्थ्य देखभाल उत्पाद।
गुएरबेट अपने विलेपिन्टे परिचालन से फार्मास्युटिकल फॉर्मूलेशन, जेनेरिक दवाएं और स्वास्थ्य देखभाल उत्पाद बनाती है। कंपनी अपने सूचीबद्ध प्राथमिक बाजारों में फार्मेसी चैनल, अस्पताल खरीदारों, स्वास्थ्य सेवा वितरकों या निर्यात ग्राहकों को आपूर्ति करती है।
- Type
- Manufacturer
- Location
- Villepinte, France
- Founded
- 1926
- Website
- guerbet.com
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, पूरक और कल्याण
- Markets
- फ़्रांस, संयुक्त राज्य, जर्मनी, जापान
Verified facts
- lei-active (green), checked 2026-08-07 GLEIF global LEI register (golden copy)
- operating-permit (green), checked 2013-10-31 EEA Industrial Emissions Portal (IED), EU-wide permit register
- domain-registered (green), checked 2026-07-28 Domain registry record
- places-goods-on-market (green), checked 2026-08-09 Registre national des producteurs (ADEME/SYDEREP), France
- registry-active-global (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-07-09 INSEE Sirene (annuaire-entreprises)
- media-mention (green), checked 2026-07-18 Radiology Business
- aeo-certified (green), checked 2026-08-07 EU AEO register (European Commission)
- 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
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)