Suppliers / Medinsa - Laboratorios Medicamentos Internacionales

Medinsa - Laboratorios Medicamentos Internacionales

Spain 212 employees Updated 9 July 2026

Medinsa - Laboratorios Medicamentos Internacionales is a finished-dose manufacturer based in Spain. It appears in 4 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), AEMPS (ES) and EDE (AE). Its GMP standing is certified by EAEU_EEC, AEMPS (ES) and EMA.

0
active US DMFs
0
valid CEPs
3
registered plants
4
filings across 3 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
Madrid, United Arab Emirates Not on file
Madrid, Spain Not on file
Torrejon De Ardoz, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 2 None
AEMPS (ES) 1 1
EDE (AE) 1 None
EAEU_EEC None 1
EMA None 1

Questions about Medinsa - Laboratorios Medicamentos Internacionales

Does Medinsa - Laboratorios Medicamentos Internacionales hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Medinsa - Laboratorios Medicamentos Internacionales. It does have 4 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Medinsa - Laboratorios Medicamentos Internacionales manufacture?
3 registered sites are on record, in United Arab Emirates and Spain (Madrid and Torrejon De Ardoz among others). Every site is listed on this page with the register it came from.
Which regulators recognise Medinsa - Laboratorios Medicamentos Internacionales's GMP?
Current GMP certificates are on record from EEC (Eurasian Economic Union), 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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Sources on this page

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