Lonza AG
Lonza AG is a drug establishment in Basel, Switzerland, registered with the US FDA under FEI 3014753648. Its registered operations are: Analytical testing. 8 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.
GMP documents matched to this site (8)
| Document | Authority | Inspection | Source |
|---|---|---|---|
GMPE-CH-1007311 GMP certificate | Competent authority of Switzerland | 10 Jul 2025 within 3-year review window | EudraGMDP |
GMPE-CH-1006613 GMP certificate | Competent authority of Switzerland | 10 Jul 2024 within 3-year review window | EudraGMDP |
GMPE-CH-1007959 GMP certificate | Competent authority of Switzerland | 10 Jul 2024 within 3-year review window | EudraGMDP |
GMPE-CH-1007428 GMP certificate | Competent authority of Switzerland | 10 Jul 2024 within 3-year review window | EudraGMDP |
GMPE-CH-1007386 GMP certificate | Competent authority of Switzerland | 10 Jul 2024 within 3-year review window | EudraGMDP |
GMPE-CH-1006253 GMP certificate | Competent authority of Switzerland | 10 Jul 2024 within 3-year review window | EudraGMDP |
GMPE-CH-1005576 GMP certificate | Competent authority of Switzerland | 31 Mar 2022 outside 3-year review window | EudraGMDP |
GMPE-CH-1005944 GMP certificate | Competent authority of Switzerland | 31 Mar 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.
Other sites registered by the same company
- Lonza AGVisp, Switzerland · API manufacture
- Lonza AGStein AG, Switzerland
- Lonza AGVisp, Switzerland · API manufacture
- Lonza Biologics Porrino SLO PORRI�O, Spain · API manufacture
- LONZA BIOLOGICS TUAS PTE. LTD.Singapore, Singapore · API manufacture
- Lonza Biologics, Inc.Portsmouth, United States · API manufacture
- Lonza Biologics, plcSlough, United Kingdom · API manufacture
- Lonza Guangzhou Pharmaceutical Ltd.Guangzhou, China · API manufacture
- Lonza Houston, IncHouston, United States · API manufacture
- Lonza Manufacturing LLCVacaville, United States · API manufacture
- Lonza Netherlands B.V.Geleen, Netherlands