Suppliers / Laboratorios Siegfried, S.A.S

Laboratorios Siegfried, S.A.S

Colombia Updated 9 July 2026

The public registers hold a second record for Laboratorios Siegfried, S.A.S. The fuller profile, with 94 active US DMFs and 40 valid CEPs, is at Siegfried. Figures on this page cover only this record.

Laboratorios Siegfried, S.A.S is a finished-dose manufacturer based in Colombia. It appears in 379 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with INHRR (VE), INVIMA (CO) and ARCSA (EC). Its GMP standing is certified by ARCSA (EC).

0
active US DMFs
0
valid CEPs
1
registered plants
379
filings across 4 regulators

Registered plants

Site FDA FEI
Bogota D.C., Colombia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
INHRR (VE) 152 None
INVIMA (CO) 146 None
ARCSA (EC) 80 1
MINSA (CR) 1 None

Questions about Laboratorios Siegfried, S.A.S

Does Laboratorios Siegfried, S.A.S hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Siegfried, S.A.S. It does have 379 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Siegfried, S.A.S manufacture?
1 registered site is on record, in Colombia (Bogota D.c.). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Siegfried, S.A.S's GMP?
Current GMP certificates are on record from ARCSA (EC). 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