Charles River Laboratories
药物制剂、仿制药和保健品。
Charles River Laboratories 通过其位于威尔明顿的工厂生产药物制剂、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
- Wilmington, United States
- Founded
- 1947
- Website
- charlesriver.com
- Categories
- 医疗保健用品, 补充剂与健康
- Markets
- 美国, 德国, 日本, 巴西
Verified facts
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- lei-active (green), checked 2026-08-08 GLEIF
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- facility-registered (green), checked 2026-08-04 US EPA Facility Registry Service
- domain-registered (green), checked 2026-08-08 Domain registry record
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)