Suppliers / Laboratorio Bagó De Chile

Laboratorio Bagó De Chile

Chile 2 duplicate records merged Updated 9 July 2026

Laboratorio Bagó De Chile is a finished-dose manufacturer based in Chile. It appears in 128 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with ISP (CL) and ARCSA (EC). Its GMP standing is certified by ISP (CL).

0
active US DMFs
0
valid CEPs
0
registered plants
128
filings across 2 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
ISP (CL) 71 1
ARCSA (EC) 57 None

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Laboratorio Bagó De Chile

Does Laboratorio Bagó De Chile hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Bagó De Chile. It does have 128 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Which regulators recognise Laboratorio Bagó De 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