Suppliers / Laboratorios Karizoo

Laboratorios Karizoo

Spain Updated 9 July 2026

Laboratorios Karizoo is a finished-dose manufacturer based in Spain. It appears in 11 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with URPL (PL) and MPA (SE). Its GMP standing is certified by EMA and AEMPS (ES).

0
active US DMFs
0
valid CEPs
2
registered plants
11
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Barcelona, Spain Not on file
Caldes De Montbui, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
URPL (PL) 8 None
MPA (SE) 3 None
EMA None 1
AEMPS (ES) None 1

Questions about Laboratorios Karizoo

Does Laboratorios Karizoo hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Karizoo. It does have 11 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Karizoo manufacture?
2 registered sites are on record, in Spain (Barcelona and Caldes De Montbui). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Karizoo's GMP?
Current GMP certificates are on record from EMA and AEMPS (ES). 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