Our Paperless GMP Software is designed for pharmaceutical, API, nutraceutical, herbal, veterinary, cosmetic, and medical device manufacturing companies that aim to strengthen compliance and streamline documentation. The software caters to small, medium, and large-scale manufacturers, including CMOs and CDMOs, who are preparing for WHO GMP, EU GMP, USFDA, MHRA, TGA, and PIC/S audits.
It is ideal for QA, QC, Production, Warehouse, Engineering, Microbiology, Packaging, and Regulatory Affairs teams responsible for maintaining data integrity, documentation accuracy, and audit readiness. Typical users include QA Managers, QC Analysts, Production Supervisors, Document Controllers, Validation Professionals, Compliance Officers, and Plant Heads.
Companies facing challenges with manual paperwork, delayed approvals, incomplete training records, recurring deviations, and paper-based batch documentation benefit the most from this solution. The software provides real-time visibility, automated workflows, ALCOA+ compliant data handling, and improved traceability across operations.
Businesses across India, the Middle East, Africa, Southeast Asia, and emerging global markets use the system to transition from manual processes to a fully digital, cloud-based, and reliable GMP environment.
