Suppliers / Genfar Desarrollo Y Manufactura

Genfar Desarrollo Y Manufactura

Colombia Updated 9 July 2026

Genfar Desarrollo Y Manufactura is a finished-dose manufacturer based in Colombia. It appears in 729 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with INHRR (VE), ARCSA (EC) and INVIMA (CO).

0
active US DMFs
0
valid CEPs
0
registered plants
729
filings across 6 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
INHRR (VE) 290 None
ARCSA (EC) 212 None
INVIMA (CO) 117 None
DIGEMAPS (DO) 97 None
MINSA (CR) 10 None
TITCK (TR) 3 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 Genfar Desarrollo Y Manufactura

Does Genfar Desarrollo Y Manufactura hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Genfar Desarrollo Y Manufactura. It does have 729 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Genfar Desarrollo Y Manufactura file?
Filings are on record with INHRR (VE), ARCSA (EC), INVIMA (CO), DIGEMAPS (DO) and 2 other regulators, 729 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