Suppliers / Siegfried Barbera S.L

Siegfried Barbera S.L

Spain 2 duplicate records merged Updated 9 July 2026

Siegfried Barbera S.L is a finished-dose manufacturer based in Spain. It appears in 31 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with MINSA (CR), ARCSA (EC) and UZPHARM (UZ). Its GMP standing is certified by ANVISA (Brazil), MFDS (Korea) and EMA, among 4 authorities. Its most recent recorded inspection, by US FDA, closed on 30 March 2023 as VAI.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
31
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 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

  • 30 March 2023 VAI US FDA
  • 11 October 2018 VAI US FDA
  • 18 July 2014 NAI US FDA

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

Registered plants

Site FDA FEI
Barbera del Valles (Barcelona), United Arab Emirates Not on file
BARCELONA, Spain Not on file
Barcelona, Spain Not on file
Barbera Del Valles, Spain Not on file
Spain, Spain 3002910506

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 13 None
ARCSA (EC) 7 None
UZPHARM (UZ) 5 None
NCELS (KZ) 4 None
DIGEMAPS (DO) 2 None
ANVISA (Brazil) None 3
MFDS (Korea) None 2
EMA None 2
AEMPS (ES) None 1

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Open risk flags

  • The most recent inspection outcome was VAI, on 30 March 2023.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates