Suppliers / Elaiapharm

Elaiapharm

France 18 employees Updated 9 July 2026

Elaiapharm is a finished-dose manufacturer based in France. It appears in 15 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), MINSA (CR) and INVIMA (CO). Its GMP standing is certified by ANSM (FR), EMA and ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
15
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Valbonne, United Arab Emirates Not on file
France, France 3005659648
VALBONNE, France Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 8 None
MINSA (CR) 6 None
INVIMA (CO) 1 None
ANSM (FR) None 3
EMA None 1
ANVISA (Brazil) None 1

Scale

Year Revenue Exports Destinations
2024 $43.2M Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Company filings
Revenue as reported