Novaqis Technologies LLP builds a unified GxP regulated-operations software platform for pharmaceutical, biotech, sterile, API and other GMP manufacturers. The suite covers document management (DMS), quality management (eQMS), learning management (LMS), laboratory information management (LIMS), InstrumentLink instrument SDK, Lab Digitize, electronic batch records (BRM), cleanroom eLog logbooks, ERP/WMS, HRMS, AuditLens audit intelligence, reporting and Nova AI, all on a single-database architecture designed to support 21 CFR Part 11, EU Annex 11 and CDSCO Revised Schedule M. It uses site-wide licensing with no per-user seat fees and supports on-premise and private cloud deployment.