BLAU FARMACEUTICA S.A.
Produttore brasiliano di fabbricazione di farmaci alopátici per uso umano
BLAU FARMACEUTICA S.A. è un produttore brasiliano specializzato nella fabbricazione di medicamentos alopáticos para uso humano, con sede a COTIA. Elencato nel registro ufficiale della Receita Federal CNPJ del Brasile; serve il mercato nazionale ed è aperto a partnership di distribuzione all'ingrosso 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
- Produzione farmaceutica
- Markets
- Brasile
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)
- 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
- tax-debt-published (red), checked 2026-09-22 Brazilian National Treasury Attorney's Office (PGFN), active federal debt register
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)