Lonza AG

Visp, SwitzerlandFEI 3002930340API manufacture registered

Lonza AG is a drug establishment in Visp, Switzerland, registered with the US FDA under FEI 3002930340. Its registered operations are: Analytical testing, API manufacture. 21 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 manufacture

GMP documents matched to this site (21)

DocumentAuthorityInspectionSource
GMPE-CH-1007646
GMP certificate
Competent authority of Switzerland26 Jun 2025
within 3-year review window
EudraGMDP
GMPE-CH-1007962
GMP certificate
Competent authority of Switzerland26 Jun 2025
within 3-year review window
EudraGMDP
GMPE-CH-1007432
GMP certificate
Competent authority of Switzerland4 Oct 2024
within 3-year review window
EudraGMDP
GMPE-CH-1007390
GMP certificate
Competent authority of Switzerland4 Oct 2024
within 3-year review window
EudraGMDP
GMPE-CH-1006689
GMP certificate
Competent authority of Switzerland4 Oct 2024
within 3-year review window
EudraGMDP
GMPE-CH-1007963
GMP certificate
Competent authority of Switzerland4 Oct 2024
within 3-year review window
EudraGMDP
GMPE-CH-1006616
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1007389
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1007431
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1005947
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1005575
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1006207
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1006617
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1006206
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPEHV-CH-1005948
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPEI-CH-1005948
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1005574
GMP certificate
Competent authority of Switzerland19 Aug 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1007310
GMP certificate
Competent authority of Switzerland5 May 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1006219
GMP certificate
Competent authority of Switzerland5 May 2022
outside 3-year review window
EudraGMDP
GMPE-CH-1005616
GMP certificate
Competent authority of Switzerland18 Dec 2020
outside 3-year review window
EudraGMDP
GMPEHV-CH-1005594
GMP certificate
Competent authority of Switzerland18 Dec 2020
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