Sumitomo Chemical Co., Ltd. Okayama Works - B0825
Planta certificada pela agência reguladora sanitária brasileira (ANVISA)
A ANVISA, órgão regulador sanitário brasileiro, possui certificado de Boas Práticas de Fabricação válido para esta planta, abrangendo insumos farmacêuticos ativos, válido até 08/01/2028. O certificado é emitido após inspeção na própria fábrica, por isso um órgão regulador estrangeiro batiza este site: produtos fabricados aqui são permitidos no mercado brasileiro. Número do processo 25351708754202357.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Japan
- Categories
- Fabricação farmacêutica
- Markets
- Japão, 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)
- debarment-clear (green), checked 2026-09-02 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-09-02 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
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)