Bayer AG
Bayer AG is a drug establishment in Bergkamen, Germany, registered with the US FDA under FEI 3002808084. Its registered operations are: Analytical testing, API manufacture. 5 EU/UK GMP certificates are matched to this site, 3 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.
GMP documents matched to this site (5)
| Document | Authority | Inspection | Source |
|---|---|---|---|
DE_NW_01_GMP_2026_0029 GMP certificate | Competent authority of Germany | 18 Jun 2026 within 3-year review window | EudraGMDP |
DE_NW_01_GMP_2025_0001 GMP certificate | Competent authority of Germany | 14 Nov 2024 within 3-year review window | EudraGMDP |
DE_NW_06_GMP_2024_0003 GMP certificate | EU competent authority | 20 Dec 2023 within 3-year review window | EudraGMDP |
DE_NW_01_GMP_2023_0015 GMP certificate | Competent authority of Germany | 16 Aug 2022 outside 3-year review window | EudraGMDP |
DE_NW_01_GMP_2024_0017 GMP certificate | Competent authority of Germany | 16 Aug 2022 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.