Suppliers / Laboratorios Leti, S.A.V

Laboratorios Leti, S.A.V

Venezuela Updated 9 July 2026

Laboratorios Leti, S.A.V is a finished-dose manufacturer based in Venezuela. It appears in 920 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with INHRR (VE), ARCSA (EC) and MINSA (CR).

0
active US DMFs
0
valid CEPs
1
registered plants
920
filings across 6 regulators

Registered plants

Site FDA FEI
MADRID, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INHRR (VE) 835 None
ARCSA (EC) 48 None
MINSA (CR) 21 None
DIGEMAPS (DO) 14 None
MPA (SE) 1 None
URPL (PL) 1 None

Questions about Laboratorios Leti, S.A.V

Does Laboratorios Leti, S.A.V hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Leti, S.A.V. It does have 920 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Leti, S.A.V manufacture?
1 registered site is on record, in Portugal (Madrid). Every site is listed on this page with the register it came from.
Where does Laboratorios Leti, S.A.V file?
Filings are on record with INHRR (VE), ARCSA (EC), MINSA (CR), DIGEMAPS (DO) and 2 other regulators, 920 in total.

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