Suppliers / Medifarma S A

Medifarma S A

Peru 2 duplicate records merged Updated 9 July 2026

Medifarma S A is a finished-dose manufacturer based in Peru. It appears in 234 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), ARCSA (EC) and INVIMA (CO). Its GMP standing is certified by INVIMA (CO).

0
active US DMFs
0
valid CEPs
3
registered plants
234
filings across 5 regulators

Registered plants

Site FDA FEI
Guarne, Colombia Not on file
San Luis Rio Colorado, Mexico Not on file
LIMA, Peru Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 89 None
ARCSA (EC) 89 None
INVIMA (CO) 45 1
MINSA (CR) 10 None
NPRA (MY) 1 None

Questions about Medifarma S A

Does Medifarma S A hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Medifarma S A. It does have 234 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Medifarma S A manufacture?
3 registered sites are on record, in Colombia, Mexico and Peru (Guarne, San Luis Rio Colorado and Lima). Every site is listed on this page with the register it came from.
Which regulators recognise Medifarma S A's GMP?
Current GMP certificates are on record from INVIMA (CO). 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