Chiesi
Preparaty farmaceutyczne, leki generyczne i produkty zdrowotne.
Chiesi produkuje preparaty farmaceutyczne, leki generyczne i produkty zdrowotne w ramach swoich oddziałów w Parmie. Firma zaopatruje kanały apteczne, nabywców szpitali, dystrybutorów opieki zdrowotnej lub klientów eksportowych na swoich notowanych rynkach głównych.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Parma, Italy
- Founded
- 1935
- Website
- chiesi.com
- Categories
- Artykuły medyczne i związane z opieką zdrowotną, Suplementy i dobre samopoczucie
- Markets
- Włochy, Stany Zjednoczone, Niemcy, Francja
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
- lei-active (green), checked 2026-08-08 GLEIF
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- registered-manufacturer (green), checked 2026-09-17 Ministero della Salute, banca dati e Repertorio dei dispositivi medici
- export-registered (green), checked 2026-07-30 EU EORI validation (European Commission)
- media-mention (green), checked 2026-07-18 Salesforce
- state-aid-sector (green), effective since 2026-02-23 Registro Nazionale degli Aiuti di Stato (rna.gov.it), open data
- vat-valid (green), checked 2026-08-08 VIES
Profiles
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- 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)