Nordmark Pharma GmbH

Uetersen, GermanyFEI 3003293533API manufacture registered

Nordmark Pharma GmbH is a drug establishment in Uetersen, Germany, registered with the US FDA under FEI 3003293533. Its registered operations are: Analytical testing, API manufacture, Labelling, Drug manufacture, Packaging. 12 EU/UK GMP certificates are matched to this site, 6 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 testingAPI manufactureLabellingDrug manufacturePackaging

GMP documents matched to this site (12)

DocumentAuthorityInspectionSource
DE_SH_01_GMP_2026_0035
GMP certificate
Competent authority of Germany10 Jul 2025
within 3-year review window
EudraGMDP
DE_SH_01_GMP_2026_0012
GMP certificate
Competent authority of Germany10 Jul 2025
within 3-year review window
EudraGMDP
DE_SH_01_GMP_2026_0036
GMP certificate
Competent authority of Germany10 Jul 2025
within 3-year review window
EudraGMDP
DE_SH_01_GMP_2026_0011
GMP certificate
Competent authority of Germany10 Jul 2025
within 3-year review window
EudraGMDP
DE_SH_01_GMP_2026_0010
GMP certificate
Competent authority of Germany10 Jul 2025
within 3-year review window
EudraGMDP
DE_SH_01_GMP_2026_0037
GMP certificate
Competent authority of Germany10 Jul 2025
within 3-year review window
EudraGMDP
DE_SH_01_GMP_2024_0012
GMP certificate
Competent authority of Germany31 Aug 2023
outside 3-year review window
EudraGMDP
DE_SH_01_GMP_2024_0013
GMP certificate
Competent authority of Germany31 Aug 2023
outside 3-year review window
EudraGMDP
DE_SH_01_GMP_2025_0022
GMP certificate
Competent authority of Germany31 Aug 2023
outside 3-year review window
EudraGMDP
DE_SH_01_GMP_2024_0014
GMP certificate
Competent authority of Germany31 Aug 2023
outside 3-year review window
EudraGMDP
DE_SH_01_GMP_2025_0021
GMP certificate
Competent authority of Germany31 Aug 2023
outside 3-year review window
EudraGMDP
DE_SH_01_GMP_2025_0020
GMP certificate
Competent authority of Germany31 Aug 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.