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).

active US DMFs

valid CEPs

registered plants 1 with an FDA FEI number

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 We do not publish the identity of any buyer.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.

Questions about Elaiapharm

Does Elaiapharm hold a US DMF or a CEP?

No active US drug master file or valid CEP is on record for Elaiapharm. It does have 15 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.

Is Elaiapharm FDA-registered?

One site operated by Elaiapharm 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.

Where does Elaiapharm manufacture?

3 registered sites are on record, in United Arab Emirates and France (Valbonne, France and Valbonne). Every site is listed on this page with the register it came from.

Which regulators recognise Elaiapharm's GMP?

Current GMP certificates are on record from ANSM (FR), EMA and ANVISA (Brazil). 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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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
Company filings: Revenue as reported