Urufarma S.A.
Uruguayaanse farmaceutische fabrikant gespecialiseerd in hormonale en oncologische producten sinds 1946
Urufarma is een in Montevideo gevestigde farmaceutische fabrikant die hormonale producten, orale anticonceptiva en oncologische medicijnen produceert voor export naar meer dan 50 landen. Het bedrijf is GLP-gecertificeerd en heeft onlangs een nieuw industrieel complex in de buurt van Carrasco Airport ingehuldigd.
- 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
- Medische en gezondheidszorgbenodigdheden, Landbouw en grondstoffen, Voertuigonderdelen en accessoires
- Markets
- Uruguay, Argentinië, Chili, Bolivia, Peru, Colombia, Mexico
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