Suppliers / LDP Laboratorios Torlan

LDP Laboratorios Torlan

Spain 62 employees Updated 9 July 2026

LDP Laboratorios Torlan is a finished-dose manufacturer based in Spain. It appears in 64 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), AEMPS (ES) and FAMHP (BE). Its GMP standing is certified by AEMPS (ES) and EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
64
filings across 7 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
Barcelona, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 38 None
AEMPS (ES) 18 2
FAMHP (BE) 2 None
NCELS (KZ) 2 None
INFARMED (PT) 2 None
UZPHARM (UZ) 1 None
EMA None 1

Questions about LDP Laboratorios Torlan

Does LDP Laboratorios Torlan hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for LDP Laboratorios Torlan. It does have 64 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does LDP Laboratorios Torlan manufacture?
2 registered sites are on record, in Spain (Barcelona among others). Every site is listed on this page with the register it came from.
Which regulators recognise LDP Laboratorios Torlan's GMP?
Current GMP certificates are on record from 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