Pfizer Ireland Pharmaceuticals Unlimited Company
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.
A ANVISA, órgão regulador sanitário brasileiro, possui certificado de Boas Práticas de Fabricação válido para esta planta, abrangendo insumos farmacêuticos ativos biológicos, válido até 20/05/2028. O certificado é emitido após inspeção na própria fábrica, por isso um órgão regulador estrangeiro batiza este site: produtos fabricados aqui são permitidos no mercado brasileiro. Número do processo 25351663731201768.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Ireland
- Categories
- Fabricação farmacêutica
- Markets
- Irlanda, Brasil
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 9 official records from 7 official sources are on file. 2 other entries are not official records: our own technical checks and searches, open directory listings, our inferences or the company's own statements. 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
- Authorised Economic Operator in the EU customs register (record type: aeo-certified) [official record; status green] Customs granted trusted-trader status after auditing its procedures. checked 2026-08-30. EU AEO register (European Commission)
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. checked 2026-09-02. OpenSanctions
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. checked 2026-09-02. OpenSanctions
- Active legal entity ID (LEI) (record type: lei-active) [official record; status green] A global identifier used in finance; an active one is renewed yearly. checked 2026-09-07. GLEIF global LEI register (golden copy)
- Listed in a source registry (record type: listed-in-registry) [official record; status amber] Listed in The Companies Registration Office – an Oifig um Chlarú Cuideachtaí; entry number 490938. Matched to this company by name only; no second anchor confirms it is the same legal entity.. Found in a named public register, not only on its own website. checked 2026-09-02. BRIS, EU business registers interconnection (e-justice.europa.eu)
- GMP certificate from a medicines agency (record type: gmp-certified) [official record; status green] A medicines regulator inspected the site and confirmed it may manufacture medicines. checked 2026-10-03. ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- 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)
- Site address listed in a government regulator's register (record type: facility-registered) [official record; status green] Shows the regulator records a site of this company at a named address. A registration is not an observation of current production. checked 2026-09-07. European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- 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 2026-09-07. Companies Registration Office (CRO), Ireland
- Annual accounts filed with the register (record type: annual-accounts-filed) [official record; status green] Indicates the company still meets its reporting duties. checked 2026-09-07. Companies Registration Office (CRO), Ireland
- On the company register (record type: registered-since) [official record; status green] Shows how long the company has been on the state register, which is hard to fake and easy to check. checked 2026-09-07. Companies Registration Office (CRO), Ireland
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)