FAES Farma
Formulazioni farmaceutiche, medicinali generici e prodotti sanitari.
FAES Farma produce formulazioni farmaceutiche, medicinali generici e prodotti sanitari dalle sue attività di Leioa. L'azienda fornisce canali farmaceutici, acquirenti ospedalieri, distributori sanitari o clienti esportatori nei mercati primari elencati.
- Type
- brand seeking distribution
- Location
- Leioa, Spain
- Founded
- 1933
- Website
- faesfarma.com
- Categories
- Forniture medicali e sanitarie, Integratori e benessere
- Markets
- Spagna, Stati Uniti, Germania, Francia
Verified facts
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- web-presence-since (green), checked 2026-08-02 Internet Archive (Wayback)
- 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
- product-authorised-for-sale (green), checked 2026-08-20 NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- registered-food-manufacturer (green), checked 2026-08-31 RGSEAA (Registro General Sanitario de Empresas Alimentarias y Alimentos, AESAN)
Profiles
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)