Novartis Pharma AG

Basel, SwitzerlandFEI 3002807772API manufacture registered

Novartis Pharma AG is a drug establishment in Basel, Switzerland, registered with the US FDA under FEI 3002807772. Its registered operations are: Analytical testing, API manufacture, Drug manufacture. 32 EU/UK GMP certificates are matched to this site, 19 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 manufactureDrug manufacture

GMP documents matched to this site (32)

DocumentAuthorityInspectionSource
GMPE-CH-1008824
GMP certificate
Competent authority of Switzerland18 Dec 2025
within 3-year review window
EudraGMDP
GMPE-CH-1008200
GMP certificate
Competent authority of Switzerland18 Dec 2025
within 3-year review window
EudraGMDP
GMPE-CH-1008395
GMP certificate
Competent authority of Switzerland18 Dec 2025
within 3-year review window
EudraGMDP
GMPEI-CH-1007602
GMP certificate
Competent authority of Switzerland14 May 2025
within 3-year review window
EudraGMDP
GMPEI-CH-1008196
GMP certificate
Competent authority of Switzerland14 May 2025
within 3-year review window
EudraGMDP
GMPEI-CH-1008394
GMP certificate
Competent authority of Switzerland14 May 2025
within 3-year review window
EudraGMDP
GMPE-CH-1006529
GMP certificate
Competent authority of Switzerland11 Sept 2024
within 3-year review window
EudraGMDP
GMPE-CH-1008194
GMP certificate
Competent authority of Switzerland11 Sept 2024
within 3-year review window
EudraGMDP
GMPE-CH-1007600
GMP certificate
Competent authority of Switzerland11 Sept 2024
within 3-year review window
EudraGMDP
GMPE-CH-1007049
GMP certificate
Competent authority of Switzerland11 Sept 2024
within 3-year review window
EudraGMDP
GMPEI-CH-1008825
GMP certificate
Competent authority of Switzerland5 Sept 2024
within 3-year review window
EudraGMDP
GMPEI-CH-1006824
GMP certificate
Competent authority of Switzerland5 Sept 2024
within 3-year review window
EudraGMDP
GMPEI-CH-1008195
GMP certificate
Competent authority of Switzerland7 Dec 2023
within 3-year review window
EudraGMDP
GMPEI-CH-1008393
GMP certificate
Competent authority of Switzerland7 Dec 2023
within 3-year review window
EudraGMDP
GMPEI-CH-1005766
GMP certificate
Competent authority of Switzerland7 Dec 2023
within 3-year review window
EudraGMDP
GMPEI-CH-1007601
GMP certificate
Competent authority of Switzerland7 Dec 2023
within 3-year review window
EudraGMDP
GMPEI-CH-1005930
GMP certificate
Competent authority of Switzerland7 Dec 2023
within 3-year review window
EudraGMDP
GMPEI-CH-1005911
GMP certificate
Competent authority of Switzerland10 Nov 2023
within 3-year review window
EudraGMDP
GMPEI-CH-1005554
GMP certificate
Competent authority of Switzerland10 Nov 2023
within 3-year review window
EudraGMDP
GMPE-CH-1005932
GMP certificate
Competent authority of Switzerland29 Sept 2023
outside 3-year review window
EudraGMDP
GMPE-CH-1007603
GMP certificate
Competent authority of Switzerland29 Sept 2023
outside 3-year review window
EudraGMDP
GMPE-CH-1005716
GMP certificate
Competent authority of Switzerland29 Sept 2023
outside 3-year review window
EudraGMDP
GMPE-CH-11007052
GMP certificate
Competent authority of Switzerland29 Sept 2023
outside 3-year review window
EudraGMDP
GMPEHV-CH-1005503
GMP certificate
Competent authority of Switzerland17 Jan 2023
outside 3-year review window
EudraGMDP
GMPEI-CH-1005503
GMP certificate
Competent authority of Switzerland17 Jan 2023
outside 3-year review window
EudraGMDP
GMPE-CH-1004605
GMP certificate
Competent authority of Switzerland17 Jan 2023
outside 3-year review window
EudraGMDP
GMPEI-CH-1005931
GMP certificate
Competent authority of Switzerland17 Jan 2023
outside 3-year review window
EudraGMDP
GMPEHV-CH-1005931
GMP certificate
Competent authority of Switzerland17 Jan 2023
outside 3-year review window
EudraGMDP
GMPEHV-CH-1005929
GMP certificate
Competent authority of Switzerland15 Apr 2021
outside 3-year review window
EudraGMDP
GMPE-CH-1004602
GMP certificate
Competent authority of Switzerland15 Apr 2021
outside 3-year review window
EudraGMDP
GMPEHV-CH-1005501
GMP certificate
Competent authority of Switzerland15 Apr 2021
outside 3-year review window
EudraGMDP
GMPEI-CH-1004603
GMP certificate
Competent authority of Switzerland24 Nov 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