Suppliers / Universal Farma, S.L

Universal Farma, S.L

Spain Updated 9 July 2026

Universal Farma, S.L is a finished-dose manufacturer based in Spain. It appears in 19 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, INFARMED (PT) and MPA (SE). Its GMP standing is certified by ANVISA (Brazil), AEMPS (ES) and EMA. Its most recent recorded inspection, by US FDA, closed on 3 September 2022 as VAI.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
19
filings across 7 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 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

  • 3 September 2022 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
GUADALAJARA, Spain Not on file
Azuqueca De Henares, Spain Not on file
Spain, Spain 3014360923

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 9 1
INFARMED (PT) 3 None
MPA (SE) 2 None
ARCSA (EC) 2 None
DIGEMAPS (DO) 1 None
JFDA (JO) 1 None
ANVISA (Brazil) None 3
AEMPS (ES) None 1

Questions about Universal Farma, S.L

Does Universal Farma, S.L hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Universal Farma, S.L. It does have 19 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Universal Farma, S.L FDA-registered?
One site operated by Universal Farma, S.L 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 Universal Farma, S.L's last inspection go?
The most recent inspection on record closed on 3 September 2022 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Universal Farma, S.L manufacture?
3 registered sites are on record, in Spain (Guadalajara, Azuqueca De Henares and Spain). Every site is listed on this page with the register it came from.
Which regulators recognise Universal Farma, S.L's GMP?
Current GMP certificates are on record from ANVISA (Brazil), AEMPS (ES) and EMA. 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 3 September 2022.

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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