Why Leading Healthcare Companies
Choose Our Scalable. Secure. Smart AI-Driven e-QMS
Our Quality Management System (e-QMS) is built to meet the real-world operational and compliance needs of regulated industries—from pharma to medical devices—empowering teams with automation, traceability, and intelligent insights.
Industry-Specific Design
Developed specifically for pharmaceutical, biotechnology, clinical research, and medical device companies, ensuring compliance with industry regulations and practices.
Fully Validated System
Our QMS complies with FDA, EMA, WHO, and ISO validation requirements, and we provide full system validation documents (IQ, OQ, PQ) to support your audits and regulatory filings.
Customizable Workflows
Flexible configuration to align with your SOPs and QMS policies. Supports single-site or multi-site operations.
Audit Trail & Traceability
Complete electronic audit trail capturing user actions, document history, approvals, and system changes.
Scalable & Modular
Start with the modules you need, and scale up as your operations expand. Suitable for startups to enterprise-level firms.
Integration Capabilities
Integrates with ERP, LIMS, eBMR, HRMS, and more.
GAMP 5 Compliance
Developed and maintained following GAMP 5 guidelines for computerized system validation and lifecycle management.
Multilingual Support & Global Access
Web-based platform with multi-language capabilities and 24/7 access from any location.
Industries We Empower
Our QMS platform serves the most regulated and innovation-driven sectors across life sciences and healthcare.
Pharmaceutical Manufacturing
Contract Research Organizations (CROs)
Clinical Trial Sites
Biotechnology Firms
Medical Device Manufacturers
Diagnostic Labs
Hospitals & Healthcare Providers
Nutraceuticals & Herbal Product Companies