PGF Urtica Sp. z o.o.
Fabricante farmacéutico polaco que abastece a redes de hospitales y farmacias.
PGF Urtica fabrica productos farmacéuticos genéricos y medicamentos hospitalarios en Wrocław. Fundada en 1991, la empresa distribuye a farmacias, adquisiciones hospitalarias y distribuidores de atención médica en Polonia y los mercados de Europa central y oriental.
- Type
- brand seeking distribution
- Location
- Wrocław, Poland
- Founded
- 1991
- Website
- pgf.com.pl
- Categories
- Suministros médicos y sanitarios, Suplementos y bienestar
- Markets
- Polonia, Chequia, Eslovaquia, Rumanía
Verified facts
- registry-activity (green), checked 2026-08-21 REGON national business register (GUS, Poland)
- domain-registered (green), checked 2026-08-11 Domain registry record
- registered-address (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- registered-since (green), checked 2010-12-23 Ministry of Finance VAT white list (Poland)
- tax-filing-active (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- public-contract-awarded (green), checked 2025-04-22 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)
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)