Suppliers / Infomed Fluids

Infomed Fluids

Romania Updated 9 July 2026

Infomed Fluids is a finished-dose manufacturer based in Romania. It appears in 71 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DPM (TN), EMA and EDE (AE). Its GMP standing is certified by NCELS (KZ). Its most recent recorded inspection, by US FDA, closed on 7 April 2023 as VAI.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
71
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
4 of 4 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 7 April 2023 VAI US FDA
  • 28 September 2018 VAI US FDA
  • 3 March 2017 VAI US FDA
  • 20 January 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
CONFORT, United Arab Emirates Not on file
Romania, Romania 3010600744
La Marsa, Tunisia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DPM (TN) 50 None
EMA 18 None
EDE (AE) 1 None
UZPHARM (UZ) 1 None
DIGEMAPS (DO) 1 None
NCELS (KZ) None 1

Questions about Infomed Fluids

Does Infomed Fluids hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Infomed Fluids. It does have 71 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Infomed Fluids FDA-registered?
One site operated by Infomed Fluids 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 Infomed Fluids's last inspection go?
The most recent inspection on record closed on 7 April 2023 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 4 inspections are on file.
Where does Infomed Fluids manufacture?
3 registered sites are on record, in United Arab Emirates, Romania and Tunisia (Confort, Romania and La Marsa). Every site is listed on this page with the register it came from.
Which regulators recognise Infomed Fluids's GMP?
Current GMP certificates are on record from NCELS (KZ). 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 7 April 2023.

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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