Suppliers / Laboratorio Chile

Laboratorio Chile

Chile Updated 9 July 2026

Laboratorio Chile is a finished-dose manufacturer based in Chile. It appears in 459 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with ISP (CL), ARCSA (EC) and DIGEMAPS (DO). Its GMP standing is certified by ISP (CL). Customs aggregates show $1.9M of exports covering 101 molecules to 6 destinations in 2024.

0
active US DMFs
0
valid CEPs
1
registered plants
459
filings across 3 regulators

Registered plants

Site FDA FEI
SANTIAGO, Chile Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ISP (CL) 369 1
ARCSA (EC) 71 None
DIGEMAPS (DO) 19 None

Scale

Year Revenue Exports Destinations
2024 Not reported $1.9M 6
2022 Not reported $3K 1

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Laboratorio Chile

Does Laboratorio Chile hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Chile. It does have 459 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Chile manufacture?
1 registered site is on record, in Chile (Santiago). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Chile's GMP?
Current GMP certificates are on record from ISP (CL). 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
Customs aggregates
Export values, molecule and destination counts