Menarini
Formulazioni farmaceutiche, medicinali generici e prodotti sanitari.
Menarini produce formulazioni farmaceutiche, farmaci generici e prodotti sanitari dalle sue sedi di Firenze. 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
- Florence, Italy
- Founded
- 1886
- Website
- menarini.com
- Categories
- Forniture medicali e sanitarie, Integratori e benessere
- Markets
- Italia, Stati Uniti, Germania, Francia
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 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
- public-subsidy-received (green), checked 2026-08-25 OpenCoesione (opencoesione.gov.it), open data on project subjects
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)