Pfizer Manufacturing Belgium NV

Puurs-Sint-Amands, BelgiumFEI 1000654629

Pfizer Manufacturing Belgium NV is a drug establishment in Puurs-Sint-Amands, Belgium, registered with the US FDA under FEI 1000654629. Its registered operations are: Analytical testing, Labelling, Drug manufacture, Packaging. 38 EU/UK GMP certificates are matched to this site, 31 inspected within the last three years.

Sources: FDA Drug Establishments Current Registration Site (checked 2 Nov 2026); EudraGMDP; MHRA GMDP. Methodology

Registered operations

Business operations this establishment declares in its FDA registration. Registration is not an approval and says nothing about EU or UK GMP status.

Analytical testingLabellingDrug manufacturePackaging

GMP documents matched to this site (38)

DocumentAuthorityInspectionSource
BE/GMP/2025/143
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/151
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/149
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/150
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/147
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/152
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/145
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/134
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/136
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/144
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/141
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/142
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/212
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/146
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/148
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/135
GMP certificate
Competent authority of Belgium22 Oct 2025
within 3-year review window
EudraGMDP
BE/GMP/2024/117
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/123
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/038
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/121
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/122
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/120
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/118
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/040
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/115
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/124
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/113
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/114
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/039
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/116
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2024/119
GMP certificate
Competent authority of Belgium21 Mar 2024
within 3-year review window
EudraGMDP
BE/GMP/2023/119
GMP certificate
Competent authority of BELGIUM6 Oct 2023
outside 3-year review window
EudraGMDP
BE/GMP/2023/085
GMP certificate
Competent authority of BELGIUM6 Oct 2023
outside 3-year review window
EudraGMDP
BE/GMP/2023/083
GMP certificate
Competent authority of BELGIUM6 Oct 2023
outside 3-year review window
EudraGMDP
BE/GMP/2023/084
GMP certificate
Competent authority of BELGIUM6 Oct 2023
outside 3-year review window
EudraGMDP
BE/GMP/2023/120
GMP certificate
Competent authority of BELGIUM6 Oct 2023
outside 3-year review window
EudraGMDP
BE/GMP/2022/100
GMP certificate
Competent authority of Belgium25 Nov 2022
outside 3-year review window
EudraGMDP
BE/GMP/2021/174
GMP certificate
Competent authority of Belgium4 Jun 2021
outside 3-year review window
EudraGMDP

A GMP document is matched to this site when its address names the site's street and its city or postcode. In our latest internal review 59 of 60 sampled matches were the right site (not yet independently reviewed; measured match quality). Check the certificate's own address before relying on it. The three-year review window is the EMA guideline default after an inspection, not an official expiry date.

What this page does not show

  • Which substances are made here: DMFs and CEPs are filed by organisations, not sites, so we do not link substances to this site.
  • Capacity, scale, price or current availability: no regulator publishes these.
  • FDA inspection classifications for this site, which are not yet linked.

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