Suppliers / Laboratorio Sanderson

Laboratorio Sanderson

Chile Updated 9 July 2026

Laboratorio Sanderson is a finished-dose manufacturer based in Chile. It appears in 308 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), MINSA (CR) and ARCSA (EC). Its GMP standing is certified by INVIMA (CO), ANVISA (Brazil) and ISP (CL).

0
active US DMFs
0
valid CEPs
3
registered plants
308
filings across 5 regulators

Registered plants

Site FDA FEI
SAN JOAQUIN, Chile Not on file
Santiago De Chile, Colombia Not on file
Santiago, Colombia Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 124 None
MINSA (CR) 78 None
ARCSA (EC) 72 None
INVIMA (CO) 18 2
ISP (CL) 16 1
ANVISA (Brazil) None 1

Questions about Laboratorio Sanderson

Does Laboratorio Sanderson hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Sanderson. It does have 308 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Sanderson manufacture?
3 registered sites are on record, in Chile and Colombia (SAN Joaquin, Santiago De Chile and Santiago). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Sanderson's GMP?
Current GMP certificates are on record from INVIMA (CO), ANVISA (Brazil) and ISP (CL). 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