Guerbet
药物制剂、仿制药和保健品。
加伯特通过其维勒班特工厂生产药物配方、仿制药和保健产品。该公司向其上市主要市场的药房渠道、医院买家、医疗保健分销商或出口客户提供服务。
- Type
- Manufacturer
- Location
- Villepinte, France
- Founded
- 1926
- Website
- guerbet.com
- Categories
- 医疗保健用品, 补充剂与健康
- Markets
- 法国, 美国, 德国, 日本
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)