Sicor De Mexico S.A. De C.V - B0372
Plant certified by the Brazilian health regulator (ANVISA)
ANVISA, the Brazilian health regulator, holds a valid Good Manufacturing Practice certificate for this plant, covering active pharmaceutical ingredients, valid until 2026-10-21. The certificate is issued after an inspection of the plant itself, which is why a foreign regulator names this site: goods made here are allowed on the Brazilian market. The certificate records the site address as AV. SAN RAFAEL NO. 35, PARQUE INDUSTRIAL LERMA, LERMA DE VILLADA, MÉXICO - 52000. Process number 25351339734202241.
- Type
- Manufacturer
- Location
- Lerma, Mexico
- Categories
- Pharmaceutical Manufacturing
- Markets
- Mexico, Brazil
Listed in a source registry
Verified facts
- gmp-certified (green), checked 2026-08-21 ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
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)