Why trust the quality of our cell therapy?
With over 20 years of dedicated research and development in biomedical solutions, we have achieved significant advancements.
Cryovida has established GMP (Good Manufacturing Practice) facilities with ISO 6 classification. We comply with the official national regulations 059-SSA1-2025, which dictate the good manufacturing practices of the pharmaceutical industry for class A laboratories. The equipment used in our laboratory guarantees production practices under ISO 5 conditions as established by current regulations.
