BLAU FARMACEUTICA S.A.
Fabricante brasileiro de fabricação de medicamentos alopáticos para uso humano
A BLAU FARMACEUTICA S.A. é uma fabricante brasileira especializada na fabricação de medicamentos alopáticos para uso humano, com sede em COTIA. Listado no registro oficial do CNPJ da Receita Federal do Brasil; atende o mercado interno e está aberto a parcerias de distribuição atacadista B2B.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- COTIA, Brazil
- Website
- https://blau.com.br
- Categories
- Fabricação farmacêutica
- Markets
- 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
- domain-registered (green), checked 2026-08-15 Domain registry record
- sanctions-clear (green), checked 2026-08-15 OpenSanctions
- debarment-clear (green), checked 2026-08-15 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-15 Mail server of the company domain
- named-by-affiliate (green), checked 2026-09-07 Official website of blau.com
- energy-market-consumer (green), effective since 2026-06-01 CCEE (Câmara de Comercialização de Energia Elétrica)
- registry-active-global (green), checked 2026-08-13 CCEE (Câmara de Comercialização de Energia Elétrica)
- registry-activity (green), checked 2026-08-15 Receita Federal (CNPJ)
- tax-debt-published (red), checked 2026-09-06 Brazilian National Treasury Attorney's Office (PGFN), active federal debt register
- directors-on-file (green), checked 2026-08-15 Receita Federal (CNPJ)
- lei-active (green), checked 2026-07-20 GLEIF
- cnpj-active (green), checked 2026-08-15 Receita Federal (CNPJ)
- registry-id-verified (green), effective since 2026-07-18 Receita Federal CNPJ lookup
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)