Urufarma S.A.
1946'dan beri hormonal ve onkolojik ürünlerde uzmanlaşmış Uruguaylı ilaç üreticisi
Urufarma, 50'den fazla ülkeye ihracat için hormonal ürünler, oral kontraseptifler ve onkolojik ilaçlar üreten Montevideo merkezli bir ilaç üreticisidir. Şirket, GLP sertifikasına sahiptir ve yakın zamanda Carrasco Havalimanı yakınlarında yeni bir sanayi kompleksinin açılışını yapmıştır.
- 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
- Tıbbi ve Sağlık Malzemeleri, Tarım ve Hammaddeler, Araç Parçaları ve Aksesuarları
- Markets
- Uruguay, Arjantin, Şili, Bolivya, Peru, Kolombiya, Meksika
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