US Pharmacia sp. z o.o.
US Pharmacia est un fabricant polonais de préparations dermatologiques et ophtalmologiques, produisant…
US Pharmacia est un fabricant polonais de préparations dermatologiques et ophtalmologiques, produisant des produits pharmaceutiques magistraux et industriels, notamment des collyres, des crèmes topiques, des solutions orales et des ingrédients pharmaceutiques composés. L'entreprise fournit aux pharmacies hospitalières, aux pharmacies de détail et aux cliniques dermatologiques spécialisées dans toute la Pologne des spécialités pharmaceutiques sous licence et fabrique certains produits sous contrat pour des distributeurs pharmaceutiques européens.
- Type
- brand seeking distribution
- Location
- Wrocław, Poland
- Founded
- 1990
- Website
- uspharmacia.pl
- Categories
- Fournitures médicales et de santé, Soins et cosmétiques
- Markets
- Pologne, Tchéquie, Slovaquie, Hongrie, Roumanie, Allemagne, Lituanie
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)