CLINICAL TRIAL MANAGEMENTACT-LIMSTM is a multi-tier, multi-user, cost-effective Laboratory Information Management System (LIMS) especially suited for pharmaceutical industry. It enables R&D and manufacturing laboratories to perform QA/QC on all inventories, keep accurate track of samples, reagents, instruments, processes and output. It provides complete and cost effective solution for implementing a paperless Pharma lab.
DG-LIMSTM is compliant with requirements and guidelines for GxP as stipulated by US EPA, US FDA and WHO. It complies with US FDA 21 CFR Part 11 requirements on electronic records and electronic signatures. It meets regulatory requirements on data security and audit trails of an experiment.
DG-LIMSTM has ICH compliant testing and method validation module along with cleaning validation support during product changeover. Other functionality such as workflow, stability, QC batch management and trend analysis tools drastically reduce time and effort of implementation, validation and support.
