Suppliers / Laboratorios Ima S.A.I.C

Laboratorios Ima S.A.I.C

Argentina Updated 9 July 2026

Laboratorios Ima S.A.I.C is a finished-dose manufacturer based in Argentina. It appears in 209 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), ARCSA (EC) and ANMAT (AR). Its GMP standing is certified by ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
1
registered plants
209
filings across 5 regulators

Registered plants

Site FDA FEI
BUENOS AIRES, Argentina Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 102 None
ARCSA (EC) 55 None
ANMAT (AR) 39 None
MINSA (CR) 12 None
INVIMA (CO) 1 None
ANVISA (Brazil) None 2

Questions about Laboratorios Ima S.A.I.C

Does Laboratorios Ima S.A.I.C hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Ima S.A.I.C. It does have 209 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Ima S.A.I.C manufacture?
1 registered site is on record, in Argentina (Buenos Aires). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Ima S.A.I.C's GMP?
Current GMP certificates are on record from ANVISA (Brazil). 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.

Comparing suppliers?

Choose your molecules and target markets. Laboratorios Ima S.A.I.C comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Abbott Laboratories Argentina also in Argentina Amarin Technologies also in Argentina Eriochem also in Argentina Glenmark Generics also in Argentina Gobbi Novag also in Argentina

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates