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), EMA and ANVISA (Brazil), 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
DIGEMAPS (DO) 2 None
MPA (SE) 2 None
INFARMED (PT) 1 None
ANSM (FR) None 13
ANVISA (Brazil) None 1
US FDA None 1

Questions about Laboratoires Expanscience

Does Laboratoires Expanscience hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratoires Expanscience. It does have 63 filings with 9 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Laboratoires Expanscience FDA-registered?
One site operated by Laboratoires Expanscience carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Laboratoires Expanscience's last inspection go?
The most recent inspection on record closed on 20 September 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 2 inspections are on file.
Where does Laboratoires Expanscience manufacture?
3 registered sites are on record, in France (Epernon and France among others). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratoires Expanscience's GMP?
Current GMP certificates are on record from ANSM (FR), EMA, ANVISA (Brazil) and US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

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

Comparable suppliers

AdhexPharma also in France Advanced Accelerator Applications also in France Aspen Notre Dame De Bondeville also in France Astrazeneca Dunkerque Production also in France Astrea Fontaine also in France

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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