Iberfar - Indústria Farmacêutica
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
IBERFAR là công ty chính của Tập đoàn Dược phẩm Bồ Đào Nha thuộc sở hữu tư nhân được thành lập vào năm 1924. Hoạt động của tập đoàn bao gồm tất cả các lĩnh vực của ngành này.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Barcarena, Portugal
- Website
- http://www.iberfar.pt/
- Categories
- Sản xuất dược phẩm
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 5 official records from 5 official sources are on file. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Legal entity ID lapsed (record type: lei-lapsed) [official record; status amber] The global finance identifier was not renewed. checked 2026-09-07. GLEIF global LEI register (golden copy)
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-08-19. INFARMED, entidades autorizadas a fabricar medicamentos (manufacturing authorisations, Portugal)
- Medicines manufacturing or import authorisation (MIA) (record type: medicines-mia-holder) [official record; status green] A medicines regulator authorises this company to manufacture and/or import medicinal products at the named site. The register lists the authorisation itself, not which products it covers, and it is not a record of trading. effective since 2026-08-15. EudraGMDP manufacturing and importation authorisation register (EMA)
- Line of business as recorded in the state register: Manufacture of pharmaceuticals (CAE 21201) (record type: registry-activity) [official record; status green] Line of business as recorded in the state register: Manufacture of pharmaceuticals (CAE 21201). Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-09-24. SICAE, Sistema de Informação da Classificação Portuguesa de Atividades Económicas (official CAE register)
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-09-10. GLEIF Global LEI record
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)