Suppliers / FAREVA Miravel

FAREVA Miravel

France Updated 9 July 2026

FAREVA Miravel is an API and finished-dose manufacturer based in France. It appears in 8 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with INVIMA (CO) and MINSA (CR). Its GMP standing is certified by ANSM (FR).

0
active US DMFs
0
valid CEPs
1
registered plants
8
filings across 2 regulators

Registered plants

Site FDA FEI
ROMAINVILLE, France Not on file

What they file, and where

Molecule Regulators Docs
Timolol SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
INVIMA (CO) 5 None
MINSA (CR) 3 None
ANSM (FR) None 14

Scale

Year Revenue Exports Destinations
2024 $9.5M 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 We do not publish the identity of any buyer.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 FAREVA Miravel

Does FAREVA Miravel hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for FAREVA Miravel. It does have 8 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does FAREVA Miravel manufacture?
1 registered site is on record, in France (Romainville). Every site is listed on this page with the register it came from.
What does FAREVA Miravel make?
1 molecule is on record against FAREVA Miravel, including Timolol. Each links through to that molecule's full manufacturer list.
Which regulators recognise FAREVA Miravel's GMP?
Current GMP certificates are on record from ANSM (FR). 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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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