Suppliers / Laboratoires Expanscience

Laboratoires Expanscience

France Updated 9 July 2026

Laboratoires Expanscience is a finished-dose manufacturer based in France. It appears in 63 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDA (EG), EMA and URPL (PL). Its GMP standing is certified by ANSM (FR), ANVISA (Brazil) and US FDA, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 20 September 2024 as VAI.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
63
filings across 9 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
2 of 2 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 20 September 2024 VAI US FDA
  • 7 August 2015 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
EPERNON, France Not on file
France, France 3011921873
EPERNON, France Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDA (EG) 27 None
EMA 22 1
URPL (PL) 6 None
MPA (SE) 2 None
DIGEMAPS (DO) 2 None
INFARMED (PT) 1 None
ANSM (FR) None 13
ANVISA (Brazil) None 1
US FDA None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 20 September 2024.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates