PRISYM Medica is the worlds only integrated label design and production software specifically developed to meet the FDA’s current 21 CFR Part 11 and GMP requirements. It can be applied to research, development, manufacturing and distribution activities that require auditable security protocols and life cycle documentation based on the GAMP ‘V’ Model.
PRISYM Medica can help in meeting GLP, GCP, GMP and ISO requirements for sample/material/product labeling and record keeping.