Suppliers / Pfizer Manufacturing Belgium

Pfizer Manufacturing Belgium

Belgium 3 duplicate records merged Updated 9 July 2026

Pfizer Manufacturing Belgium is a finished-dose manufacturer based in Belgium. It appears in 39 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with MINSA (CR), INVIMA (CO) and ARCSA (EC). Its GMP standing is certified by ANVISA (Brazil), MFDS (Korea) and EAEU_EEC, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 22 June 2022 as VAI.

0
active US DMFs
0
valid CEPs
6
registered plants 1 with an FDA FEI number
39
filings across 6 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
5 of 5 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 22 June 2022 VAI US FDA
  • 16 November 2017 NAI US FDA
  • 30 June 2015 VAI US FDA
  • 18 March 2014 NAI US FDA
  • 23 September 2011 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Puurs Sint Amands, United Arab Emirates Not on file
Puurs, United Arab Emirates Not on file
PUURS, United Arab Emirates Not on file
Puurs, Belgium Not on file
PUURS-SINT-AMANDS, Belgium Not on file
Belgium, Belgium 1000654629

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 13 None
INVIMA (CO) 8 None
ARCSA (EC) 6 None
BOMRA (BW) 6 None
NAFDAC (NG) 5 1
SFDA (Saudi Arabia) 1 None
ANVISA (Brazil) None 4
MFDS (Korea) None 2
EAEU_EEC None 2

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Open risk flags

  • The most recent inspection outcome was VAI, on 22 June 2022.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates