Suppliers / Qualipharm Laboratorio Farmaceutico

Qualipharm Laboratorio Farmaceutico

Ecuador Updated 9 July 2026

Qualipharm Laboratorio Farmaceutico is a finished-dose manufacturer based in Ecuador. It appears in 377 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by ARCSA (EC).

0
active US DMFs
0
valid CEPs
0
registered plants
377
filings across 1 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 377 2

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 Qualipharm Laboratorio Farmaceutico

Does Qualipharm Laboratorio Farmaceutico hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Qualipharm Laboratorio Farmaceutico. It does have 377 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Which regulators recognise Qualipharm Laboratorio Farmaceutico's GMP?
Current GMP certificates are on record from ARCSA (EC). 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