Neuca SA
Líder del mercado en distribución farmacéutica y servicios de logística sanitaria.
Neuca SA distribuye un amplio portafolio de medicamentos recetados y equipos médicos a farmacias independientes. La empresa opera redes logísticas de temperatura controlada de alta precisión en todo el país. Sus rutas de entrega diarias aseguran el acceso farmacéutico a millones de pacientes.
- Type
- distributor seeking brands
- Location
- Torun, Poland
- Founded
- 1990
- Website
- neuca.pl
- Categories
- Suministros médicos y sanitarios
- Markets
- Polonia
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
- web-presence-since (green), checked 2026-08-04 Internet Archive (Wayback)
- registry-activity (green), checked 2026-08-21 REGON national business register (GUS, Poland)
- directors-on-file (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- registered-address (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- registered-since (green), checked 1994-04-01 Ministry of Finance VAT white list (Poland)
- public-contract-awarded (green), checked 2026-08-20 TED (Tenders Electronic Daily), EU public procurement award notices Aquí la adjudicación lleva además una comprobación ajena: en la UE y el EEE el comprador público debe excluir a los licitadores condenados por fraude, corrupción o blanqueo, y a aquellos con deudas tributarias o de cotizaciones establecidas por resolución firme. Directive 2014/24/EU, Article 57 (exclusion grounds)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
Claimed certifications
- 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)