Suppliers / Laboratórios Richmond S.A.C.I.F

Laboratórios Richmond S.A.C.I.F

Argentina 2 duplicate records merged Updated 9 July 2026

Laboratórios Richmond S.A.C.I.F is a finished-dose manufacturer based in Argentina. It appears in 132 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with ANMAT (AR), INVIMA (CO) and ARCSA (EC). Its GMP standing is certified by INVIMA (CO).

0
active US DMFs
0
valid CEPs
2
registered plants
132
filings across 5 regulators

Registered plants

Site FDA FEI
BUENOS AIRES, Argentina Not on file
Pilar, Provincia Buenos Aires, Colombia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ANMAT (AR) 73 None
INVIMA (CO) 32 1
ARCSA (EC) 14 None
DPM (TN) 12 None
COFEPRIS (MX) 1 None

Questions about Laboratórios Richmond S.A.C.I.F

Does Laboratórios Richmond S.A.C.I.F hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratórios Richmond S.A.C.I.F. It does have 132 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratórios Richmond S.A.C.I.F manufacture?
2 registered sites are on record, in Argentina and Colombia (Buenos Aires and Pilar, Provincia Buenos Aires). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratórios Richmond S.A.C.I.F'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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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