US Pharmacia sp. z o.o.
US Pharmacia è un produttore polacco di preparati dermatologici e oftalmologici, prod…
US Pharmacia è un produttore polacco di preparati dermatologici e oftalmologici, che produce prodotti farmaceutici magistrali e industriali tra cui colliri, creme topiche, soluzioni orali e ingredienti farmaceutici composti. L'azienda fornisce farmacie ospedaliere, farmacie al dettaglio e cliniche dermatologiche specializzate in tutta la Polonia con specialità farmaceutiche autorizzate e produce alcuni prodotti sotto contratto per i distributori farmaceutici europei.
- Type
- brand seeking distribution
- Location
- Wrocław, Poland
- Founded
- 1990
- Website
- uspharmacia.pl
- Categories
- Forniture medicali e sanitarie, Skincare e cosmetici
- Markets
- Polonia, Cechia, Slovacchia, Ungheria, Romania, Germania, Lituania
Verified facts
- vat-valid (green), checked 2026-08-01 VIES (European Commission)
- registered-units (green), checked 2026-08-21 REGON national business register (GUS, Poland)
- registry-activity (green), checked 2026-08-21 REGON national business register (GUS, Poland)
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- domain-registered (green), checked 2026-08-13 Domain registry record
- registered-address (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- registered-since (green), checked 1996-09-16 Ministry of Finance VAT white list (Poland)
- tax-filing-active (green), checked 2026-08-20 Ministry of Finance VAT white list (Poland)
- gmp-certified (green), checked 2023-10-20 EudraGMDP, EU register of GMP certificates (EMA)
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)