Shevan shik

Unlike any other generic LIMS product, Qualis LIMS is a powerful enterprise-scale LIMS developed using a strong framework and is fully configurable and customizable for regulated pharmaceutical QA/QC, R&D and analytical development environment. Qualis LIMS covers all the workflow processes within a typical regulated laboratory. It addresses several pain points of the industry and saves >50% of the time and human effort with respect to data capture, review and approvals. It addresses GLP and 21 CFR Part 11/ EudraLex Annex 11 guidelines ensuring that the Organization using it in compliance to the norms.