Laboratorios Cinfa
自 1969 年以来一直是西班牙领先的仿制药制造商，总部位于纳瓦拉
Laboratorios Cinfa 是一家领先的西班牙制药公司，于 1969 年在纳瓦拉成立，致力于开发、制造和营销仿制药和非处方药产品。拥有两座总面积 70,000 平方米的生产工厂，遍布超过 27 个国家。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Olloki, Spain
- Website
- https://www.cinfa.com
- Categories
- 药品制造
- Markets
- 西班牙
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)