Urufarma S.A.
Urugwajski producent farmaceutyków specjalizujący się w produktach hormonalnych i onkologicznych od 1946 roku
Urufarma to producent farmaceutyczny z siedzibą w Montevideo, produkujący produkty hormonalne, doustne środki antykoncepcyjne i leki onkologiczne na eksport do ponad 50 krajów. Firma posiada certyfikat GLP, a niedawno otworzyła nowy kompleks przemysłowy w pobliżu lotniska Carrasco.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Montevideo, Uruguay
- Founded
- 1946
- Website
- urufarma.com.uy
- Categories
- Artykuły medyczne i związane z opieką zdrowotną, Rolnictwo i surowce, Części i akcesoria do pojazdów
- Markets
- Urugwaj, Argentyna, Chile, Boliwia, Peru, Kolumbia, Meksyk
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- product-authorised-for-sale (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- debarment-clear (green), checked 2026-08-12 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-12 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
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)
- Vehicle parts affecting safety sold in Europe generally require UNECE type approval (E-mark). UNECE