Laboratorios Cinfa
1969'dan bu yana Navarra'da bulunan lider İspanyol jenerik ilaç üreticisi
Laboratorios Cinfa, 1969 yılında Navarra'da kurulmuş, jenerik ilaçlar ve OTC ürünleri geliştiren, üreten ve pazarlayan lider bir İspanyol ilaç şirketidir. Toplam 70.000 m2 alana sahip iki üretim tesisiyle 27'den fazla ülkede faaliyet göstermektedir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Olloki, Spain
- Website
- https://www.cinfa.com
- Categories
- İlaç Üretimi
- Markets
- İspanya
Listed in a source registry
Farmaindustria / ICEX
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
- 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
- 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
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- product-authorised-for-sale (green), checked 2026-08-21 Ministry of Health of Armenia, State Register of Medicinal Products (pharm.am)
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- 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)
- lei-active (green), checked 2026-08-16 GLEIF global LEI register (golden copy)
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)