BLAU FARMACEUTICA S.A.
Braziliaanse fabrikant van allopathische geneesmiddelen voor menselijk gebruik
BLAU FARMACEUTICA S.A. is een Braziliaanse fabrikant gespecialiseerd in de vervaardiging van allopathische geneesmiddelen voor menselijk gebruik, gevestigd in COTIA. Vermeld in het officiële IRS CNPJ-register van Brazilië; bedient de binnenlandse markt en staat open voor B2B-groothandelsdistributiepartnerschappen.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- COTIA, Brazil
- Website
- https://blau.com.br
- Categories
- Farmaceutische productie
- Markets
- Brazilië
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)