Drogueria INTI S.A.
Drogueria INTI S.A. produceert generieke geneesmiddelen voor regionale B2B-kanalen.
Drogueria INTI S.A. produceert generieke medicijnen, OTC-producten en farmaceutische formuleringen in La Paz. Het bedrijf, opgericht in 1936, levert aan apotheken, ziekenhuizen, aanbestedingen en distributeurs in BO, PE, CL, AR en aanverwante exportmarkten.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- La Paz, Bolivia
- Founded
- 1936
- Website
- inti.com.bo
- Categories
- Medische en gezondheidszorgbenodigdheden
- Markets
- Bolivia, Peru, Chili, Argentinië
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
- corporate-mail-on-domain (green), checked 2026-08-06 Mail server of the company domain
- product-authorised-for-sale (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
- registered-manufacturer (green), checked 2026-08-22 Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
- debarment-clear (green), checked 2026-08-06 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-06 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
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)