Suppliers / Laboratorios MAYMÓ

Laboratorios MAYMÓ

Spain 74 employees Updated 9 July 2026

Laboratorios MAYMÓ is a finished-dose manufacturer based in Spain. It appears in 12 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with DKMA (DK) and URPL (PL). Its GMP standing is certified by AEMPS (ES) and EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
12
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
Castellbisbal, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DKMA (DK) 8 None
URPL (PL) 4 None
AEMPS (ES) None 1
EMA None 1

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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