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), EAEU_EEC and MFDS (Korea), 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, United Arab Emirates Not on file
Puurs Sint Amands, 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
EAEU_EEC None 2
MFDS (Korea) None 2

Questions about Pfizer Manufacturing Belgium

Does Pfizer Manufacturing Belgium hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Pfizer Manufacturing Belgium. It does have 39 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Pfizer Manufacturing Belgium FDA-registered?
One site operated by Pfizer Manufacturing Belgium carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Pfizer Manufacturing Belgium's last inspection go?
The most recent inspection on record closed on 22 June 2022 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 5 inspections are on file.
Where does Pfizer Manufacturing Belgium manufacture?
6 registered sites are on record, in United Arab Emirates and Belgium (Puurs, Puurs Sint Amands and Puurs among others). Every site is listed on this page with the register it came from.
Which regulators recognise Pfizer Manufacturing Belgium's GMP?
Current GMP certificates are on record from ANVISA (Brazil), EEC (Eurasian Economic Union), MFDS (Korea) and NAFDAC (NG). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

Comparing suppliers?

Choose your molecules and target markets. Pfizer Manufacturing Belgium comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Open risk flags

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

Comparable suppliers

Baxter SA-NV also in Belgium Benechim also in Belgium Besins Manufacturing Belgium also in Belgium Catalent Belgium also in Belgium Cenexi - Laboratoires Thissen S. A also in Belgium

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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