Suppliers / Laboratorios Alcala Farma, S.L

Laboratorios Alcala Farma, S.L

Spain 123 employees Updated 9 July 2026

Laboratorios Alcala Farma, S.L is a finished-dose manufacturer based in Spain. It appears in 16 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), ARCSA (EC) and UZPHARM (UZ). Its GMP standing is certified by EAEU_EEC, AEMPS (ES) and EMA, among 4 authorities.

0
active US DMFs
0
valid CEPs
3
registered plants
16
filings across 4 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, Spain Not on file
Guadalajara, Spain Not on file
Alcala De Henares, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 6 None
ARCSA (EC) 5 None
UZPHARM (UZ) 3 None
MINSA (CR) 2 None
EAEU_EEC None 2
AEMPS (ES) None 2
EMA None 1
NCELS (KZ) None 1

Questions about Laboratorios Alcala Farma, S.L

Does Laboratorios Alcala Farma, S.L hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Alcala Farma, S.L. It does have 16 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Alcala Farma, S.L manufacture?
3 registered sites are on record, in Spain (Madrid, Guadalajara and Alcala De Henares). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Alcala Farma, S.L's GMP?
Current GMP certificates are on record from EEC (Eurasian Economic Union), AEMPS (ES), EMA and NCELS (KZ). 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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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