Lonza AG

Stein AG, SwitzerlandFEI 3016502617

Lonza AG is a drug establishment in Stein AG, Switzerland, registered with the US FDA under FEI 3016502617. Its registered operations are: Analytical testing, Drug manufacture. 10 EU/UK GMP certificates are matched to this site, 4 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 testingDrug manufacture

GMP documents matched to this site (10)

DocumentAuthorityInspectionSource
GMPE-CH-1007960
GMP certificate
Competent authority of Switzerland9 Aug 2024
within 3-year review window
EudraGMDP
GMPE-CH-1007387
GMP certificate
Competent authority of Switzerland9 Aug 2024
within 3-year review window
EudraGMDP
GMPE-CH-1007429
GMP certificate
Competent authority of Switzerland9 Aug 2024
within 3-year review window
EudraGMDP
GMPE-CH-1007312
GMP certificate
Competent authority of Switzerland9 Aug 2024
within 3-year review window
EudraGMDP
GMPE-CH-1006614
GMP certificate
Competent authority of Switzerland21 Jul 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1006220
GMP certificate
Competent authority of Switzerland21 Jul 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1005577
GMP certificate
Competent authority of Switzerland21 Jul 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1005945
GMP certificate
Competent authority of Switzerland21 Jul 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1006204
GMP certificate
Competent authority of Switzerland21 Jul 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1005615
GMP certificate
Competent authority of Switzerland21 Jul 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