Drogueria INTI S.A.
Drogueria INTI S.A. は、地域の B2B チャネル向けにジェネリック医薬品を製造しています。
Drogueria INTI S.A. は、ラパスでジェネリック医薬品、OTC 製品、医薬品製剤を製造しています。 1936 年に設立された同社は、BO、PE、CL、AR および関連輸出市場の薬局、病院、入札、販売代理店に製品を供給しています。
- 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
- 医療およびヘルスケア用品
- Markets
- ボリビア, ペルー, チリ, アルゼンチン
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)