Catalent
Formulazioni farmaceutiche, medicinali generici e prodotti sanitari.
Catalent produce formulazioni farmaceutiche, medicinali generici e prodotti sanitari dalle sue attività nel Somerset. L'azienda fornisce canali farmaceutici, acquirenti ospedalieri, distributori sanitari o clienti esportatori nei mercati primari elencati.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Somerset, United States
- Founded
- 2007
- Website
- catalent.com
- Categories
- Forniture medicali e sanitarie, Integratori e benessere
- Markets
- Stati Uniti, Germania, Giappone, Brasile
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
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
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- lei-lapsed (amber), checked 2026-08-08 GLEIF
- fda-registered (green), checked 2026-08-08 FDA
- fda-contract-manufacturer (green), checked 2026-08-08 FDA
- certificate-page-on-site (amber), checked 2026-09-18 Company's own certification page
- industrial-permit (green), checked 2026-08-23 ECHO, Enforcement and Compliance History Online (U.S. Environmental Protection Agency)
- facility-registered (green), checked 2026-08-04 US EPA Facility Registry Service
Claimed certifications, not confirmed by us
- 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)