LABORATORIO TEUTO BRASILEIRO S/A
Braziliaanse fabrikant van allopathische geneesmiddelen voor menselijk gebruik
LABORATORIO TEUTO BRASILEIRO S/A is een Braziliaanse fabrikant gespecialiseerd in de productie van allopathische geneesmiddelen voor menselijk gebruik, gevestigd in ANAPOLIS. 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
- ANAPOLIS, Brazil
- Website
- https://teuto.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
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- domain-registered (green), checked 2026-08-02 Domain registry record
- energy-market-consumer (green), effective since 2026-08-01 CCEE (Câmara de Comercialização de Energia Elétrica)
- registry-active-global (green), checked 2026-08-13 CCEE (Câmara de Comercialização de Energia Elétrica)
- cnpj-active (green), checked 2026-07-20 Receita Federal (CNPJ)
- registry-activity (green), checked 2026-07-20 Receita Federal (CNPJ)
- directors-on-file (green), checked 2026-07-20 Receita Federal (CNPJ)
- registry-id-verified (green), checked 2026-08-13 CCEE (Câmara de Comercialização de Energia Elétrica)
- development-project-financed (green), checked 2026-08-28 BNDES, Banco Nacional de Desenvolvimento Econômico e Social, Portal de Dados Abertos (operações não automáticas)
- 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)