Cryovida currently has GMP (Good Manufacturing Practice) facilities, ISO 6 classification, that comply with the OFFICIAL MEXICAN STANDARD (NOM) 059-SSA1-2025 which establishes the good manufacturing practices of the pharmaceutical industry regarding class A laboratories. Meanwhile, the equipment in the cell bank complies with the production practices and conditions of ISO 5 as established by the current regulations.
Therefore, the highest quality and production control is achieved. This is supported by third party laboratories approved by COFEPRIS. We are the only laboratory that has the three existing permits regarding the management and development of regenerative medicine based on the extraction, expansion and application of Mesenchymal Stem Cells.