ACM PHARMA

BELLEGARDE, FranceFEI 3004177283

ACM PHARMA is a drug establishment in BELLEGARDE, France, registered with the US FDA under FEI 3004177283. Its registered operations are: Analytical testing. 7 EU/UK GMP certificates are matched to this site, 5 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 testing

GMP documents matched to this site (7)

DocumentAuthorityInspectionSource
24/008101
GMP certificate
Competent authority of France15 May 2024
within 3-year review window
EudraGMDP
2024_HPF_FR_132
GMP certificate
Competent authority of France24 Jan 2024
within 3-year review window
EudraGMDP
2024_HPF_FR_133
GMP certificate
Competent authority of France24 Jan 2024
within 3-year review window
EudraGMDP
2024_HPF_FR_085
GMP certificate
Competent authority of France24 Jan 2024
within 3-year review window
EudraGMDP
2024_HPF_FR_084
GMP certificate
Competent authority of France24 Jan 2024
within 3-year review window
EudraGMDP
23-343437
GMP certificate
Competent authority of FRANCE23 Jan 2018
outside 3-year review window
EudraGMDP
18/218244
GMP certificate
Competent authority of France23 Jan 2018
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.