BLAU FARMACEUTICA S.A.
Nhà sản xuất Brazil sản xuất thuốc chữa bệnh cho người sử dụng
BLAU FARMACEUTICA S.A. là nhà sản xuất Brazil chuyên sản xuất thuốc chữa bệnh cho người sử dụng, có trụ sở tại COTIA. Được liệt kê trong cơ quan đăng ký CNPJ liên bang Receita chính thức của Brazil; phục vụ thị trường nội địa và mở cửa cho các đối tác phân phối bán buôn 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
- Sản xuất dược phẩm
- Markets
- Brazil
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)