Janssen Pharmaceutica NV

Beerse, BelgiumFEI 3002807336

Janssen Pharmaceutica NV is a drug establishment in Beerse, Belgium, registered with the US FDA under FEI 3002807336. Its registered operations are: Analytical testing, Labelling, Drug manufacture, Packaging. 10 EU/UK GMP certificates are matched to this site, 8 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 (10)

DocumentAuthorityInspectionSource
BE/GMP/2026/057
GMP certificate
Competent authority of Belgium5 Jun 2026
within 3-year review window
EudraGMDP
BE/GMP/2026/026
GMP certificate
Competent authority of Belgium25 Feb 2026
within 3-year review window
EudraGMDP
BE/GMP/2026/027
GMP certificate
Competent authority of Belgium25 Feb 2026
within 3-year review window
EudraGMDP
BE/GMP/2025/211
GMP certificate
Competent authority of Belgium4 Nov 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/120
GMP certificate
Competent authority of Belgium4 Nov 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/084
GMP certificate
Competent authority of Belgium12 May 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/047
GMP certificate
Competent authority of Belgium30 Apr 2025
within 3-year review window
EudraGMDP
BE/GMP/2025/029
GMP certificate
Competent authority of Belgium12 Mar 2025
within 3-year review window
EudraGMDP
BE/GMP/2023/058
GMP certificate
Competent authority of Belgium31 Mar 2023
outside 3-year review window
EudraGMDP
BE/GMP/2023/059
GMP certificate
Competent authority of BELGIUM31 Mar 2023
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.

Other sites registered by the same company