Cilag AG

Schaffhausen, SwitzerlandFEI 3002806695API manufacture registered

Cilag AG is a drug establishment in Schaffhausen, Switzerland, registered with the US FDA under FEI 3002806695. Its registered operations are: Analytical testing, API manufacture, Labelling, Drug manufacture, Packaging. 8 EU/UK GMP certificates are matched to this site, 8 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 manufactureLabellingDrug manufacturePackaging

GMP documents matched to this site (8)

DocumentAuthorityInspectionSource
GMPEHV-CH-1008292
GMP certificate
Competent authority of Switzerland21 Nov 2025
within 3-year review window
EudraGMDP
GMPEI-CH-1008292
GMP certificate
Competent authority of Switzerland21 Nov 2025
within 3-year review window
EudraGMDP
GMPEHV-CH-1006932
GMP certificate
Competent authority of Switzerland22 Nov 2024
within 3-year review window
EudraGMDP
GMPEI-CH-1006932
GMP certificate
Competent authority of Switzerland22 Nov 2024
within 3-year review window
EudraGMDP
GMPEHV-CH-1007168
GMP certificate
Competent authority of Switzerland22 Nov 2024
within 3-year review window
EudraGMDP
GMPEI-CH-1007168
GMP certificate
Competent authority of Switzerland22 Nov 2024
within 3-year review window
EudraGMDP
GMPEI-CH-1005342
GMP certificate
Competent authority of Switzerland17 Nov 2023
within 3-year review window
EudraGMDP
GMPEHV-CH-1005342
GMP certificate
Competent authority of Switzerland17 Nov 2023
within 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