Providing analytical testing services to meet the research and
development challenges of the pharmaceutical industry

Good Laboratory Practice (GLP)

PROTEINA has built a GLP system that meets the U.S. FDA’s GLP criteria (21 CFR Part 58).
This means that non-clinical trials that are carried out through PROTEINA services can be submitted to the FDA.
PROTEINA’s electronic quality management system (QMS) ensures all relevant documentation is digitally preserved and
that all appropriate employees receive relevant training