Suppliers / Laboratorios Cryopharma, S.A. de C.V

Laboratorios Cryopharma, S.A. de C.V

Mexico Updated 9 July 2026

Laboratorios Cryopharma, S.A. de C.V is a finished-dose manufacturer based in Mexico. It appears in 2 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by COFEPRIS (MX).

0
active US DMFs
0
valid CEPs
2
registered plants
2
filings across 1 regulators

Registered plants

Site FDA FEI
Álvaro Obregón, Mexico Not on file
Tlajomulco de Zúñiga, Mexico Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
COFEPRIS (MX) 2 4

Questions about Laboratorios Cryopharma, S.A. de C.V

Does Laboratorios Cryopharma, S.A. de C.V hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Cryopharma, S.A. de C.V. It does have 2 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Cryopharma, S.A. de C.V manufacture?
2 registered sites are on record, in Mexico (Álvaro Obregón and Tlajomulco De Zúñiga). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorios Cryopharma, S.A. de C.V's GMP?
Current GMP certificates are on record from COFEPRIS (MX). 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