Suppliers / Vicrofer

Vicrofer

Argentina Updated 9 July 2026

Vicrofer is a finished-dose manufacturer based in Argentina. It appears in 7 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO) and ARCSA (EC).

0
active US DMFs
0
valid CEPs
0
registered plants
7
filings across 2 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 6 None
ARCSA (EC) 1 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 Vicrofer

Does Vicrofer hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Vicrofer. It does have 7 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Vicrofer file?
Filings are on record with DIGEMAPS (DO) and ARCSA (EC), 7 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