Suppliers / Syntofarma S A

Syntofarma S A

Colombia Updated 9 July 2026

Syntofarma S A is a finished-dose manufacturer based in Colombia. It appears in 747 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), INVIMA (CO) and ARCSA (EC).

0
active US DMFs
0
valid CEPs
0
registered plants
747
filings across 4 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 540 None
INVIMA (CO) 137 None
ARCSA (EC) 56 None
MINSA (CR) 14 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 Syntofarma S A

Does Syntofarma S A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Syntofarma S A. It does have 747 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Syntofarma S A file?
Filings are on record with DIGEMAPS (DO), INVIMA (CO), ARCSA (EC) and MINSA (CR), 747 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