Suppliers / Laboratorios Synthesis, S.A.S

Laboratorios Synthesis, S.A.S

Colombia Updated 9 July 2026

Laboratorios Synthesis, S.A.S is a finished-dose manufacturer based in Colombia. It appears in 92 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with INVIMA (CO), ARCSA (EC) and MINSA (CR). Its GMP standing is certified by HSA (SG).

0
active US DMFs
0
valid CEPs
0
registered plants
92
filings across 4 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
INVIMA (CO) 33 None
ARCSA (EC) 30 None
MINSA (CR) 17 None
DIGEMAPS (DO) 12 None
HSA (SG) None 2

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 Laboratorios Synthesis, S.A.S

Does Laboratorios Synthesis, S.A.S hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Synthesis, S.A.S. It does have 92 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Which regulators recognise Laboratorios Synthesis, S.A.S's GMP?
Current GMP certificates are on record from HSA (SG). 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 Synthesis, S.A.S comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

C.I. Farmacapsulas also in Colombia Laboratorio Profesional also in Colombia Laboratorios Bussie S A also in Colombia Laboratorios Chalver De Colombia, S. A also in Colombia Laboratorios Ecar S A also in Colombia

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