PGF Urtica Sp. z o.o.
Produttore farmaceutico polacco che fornisce reti di ospedali e farmacie.
PGF Urtica produce farmaci generici e medicinali ospedalieri a Breslavia. Fondata nel 1991, l'azienda distribuisce a farmacie, approvvigionamenti ospedalieri e distributori sanitari in tutta la Polonia e nei mercati CEE.
- Type
- brand seeking distribution
- Location
- Wrocław, Poland
- Founded
- 1991
- Website
- pgf.com.pl
- Categories
- Forniture medicali e sanitarie, Integratori e benessere
- Markets
- Polonia, Cechia, Slovacchia, Romania
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 Qui l'aggiudicazione porta con sé anche un controllo altrui: nell'UE e nello SEE la stazione appaltante deve escludere gli operatori condannati per frode, corruzione o riciclaggio e quelli con debiti fiscali o contributivi accertati con decisione definitiva. 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)