Chugai Pharma Manufacturing Co., Ltd.
Planta certificada por el regulador sanitario brasileño (ANVISA)
ANVISA, regulador sanitario brasileño, posee para esta planta un certificado de Buenas Prácticas de Fabricación válido, que abarca ingredientes farmacéuticos activos biológicos, válido hasta el 29-07-2028. El certificado se emite después de una inspección de la propia planta, razón por la cual un regulador extranjero nombra este sitio: los productos fabricados aquí están permitidos en el mercado brasileño. Número de trámite 25351670180201799.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Japan
- Categories
- Fabricación farmacéutica
- Markets
- Japón, Brasil
Listed in a source registry
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
- gmp-certified (green), checked 2026-08-21 ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- registered-manufacturer (green), checked 2026-08-21 Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- sanctions-clear (green), checked 2026-09-01 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-09-01 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- registry-id-verified (green), checked 2026-09-22 gBizINFO (Ministry of Economy, Trade and Industry), government-held corporate data
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)