iQuaLiMS — LIMS
Sample & batch management, OOS investigations and specifications.
Pharma software cannot cut corners. Every workflow we build carries traceability, electronic signatures and audit trails aligned with 21 CFR Part 11, EU Annex 11, Schedule M and ALCOA+ principles.
From the QC lab to API production, our platforms replace paper with validated, inspection-ready digital records.
Two products covering the lab and the plant.
Sample & batch management, OOS investigations and specifications.
Change control, CAPA, incidents and document management.
Calibration, preventive maintenance and instrument integration.
Training, certification and granular user access management.
Batch production, procurement and dispatch for API manufacturing.
Dashboards for usage, sample analysis and compliance.
Compliance-first software for the pharmaceutical industry: iQuaLiMS for laboratory and quality management, and PharmaAPI ERP for active pharmaceutical ingredient manufacturing — validated to 21 CFR Part 11, EU Annex 11 and ALCOA+.
Core capabilities include iQuaLiMS — LIMS, eQMS, CPMS & Instruments, LMS & UAM — all in one integrated system.
Yes. We adapt it to your exact workflows and integrate with your existing tools. Inspection-ready records at any moment.
Book a demo and our Rajkot-based team will map Pharma Software to your requirements, then plan a phased rollout with training and support.
Book a walkthrough of iQuaLiMS and PharmaAPI ERP for your facility.