Fareva Pau

IDRON, FranceFEI 3002806390

Fareva Pau is a drug establishment in IDRON, France, registered with the US FDA under FEI 3002806390. Its registered operations are: Analytical testing, Drug manufacture, Sterilisation. 6 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 manufactureSterilisation

GMP documents matched to this site (6)

DocumentAuthorityInspectionSource
2025_HPF_FR_041
GMP certificate
Competent authority of France17 Jan 2025
within 3-year review window
EudraGMDP
2025_HPF_FR_042
GMP certificate
Competent authority of France17 Jan 2025
within 3-year review window
EudraGMDP
2024_HPF_FR_168
GMP certificate
Competent authority of France13 Sept 2024
within 3-year review window
EudraGMDP
2024_HPF_FR_167
GMP certificate
Competent authority of France13 Sept 2024
within 3-year review window
EudraGMDP
2021_HPF_FR_091_NAB_P_2024
GMP certificate
Competent authority of France12 Mar 2021
outside 3-year review window
EudraGMDP
2021_HPF_FR_092_NAB_P_2024
GMP certificate
Competent authority of France12 Mar 2021
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.