Charles River Laboratories
Formulazioni farmaceutiche, medicinali generici e prodotti sanitari.
Charles River Laboratories produce formulazioni farmaceutiche, medicinali generici e prodotti sanitari dalle sue attività a Wilmington. L'azienda fornisce canali farmaceutici, acquirenti ospedalieri, distributori sanitari o clienti esportatori nei mercati primari elencati.
- Type
- brand seeking distribution
- Location
- Wilmington, United States
- Founded
- 1947
- Website
- charlesriver.com
- Categories
- Forniture medicali e sanitarie, Integratori e benessere
- Markets
- Stati Uniti, Germania, Giappone, Brasile
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- facility-registered (green), checked 2026-08-07 US EPA Facility Registry Service (national combined file)
- industrial-permit (green), checked 2026-08-23 ECHO, Enforcement and Compliance History Online (U.S. Environmental Protection Agency)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
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)