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It is a framework used to design, validate, and maintain computerized systems in regulated industries.

Our GAMP-compliant automation solutions help pharmaceutical, biotechnology, medical device, and life sciences manufacturers implement validated, reliable, and regulatory-compliant computerized systems. Designed in accordance with GAMP 5 principles, our solutions support data integrity, process efficiency, and full compliance with global regulatory requirements.

Whether you are deploying a new automation system or upgrading an existing facility, we provide complete lifecycle support—from system design and validation to commissioning and ongoing maintenance.


Our GAMP Solutions include:

Computer System Validation (CSV)

We deliver comprehensive validation services to ensure computerized systems operate as intended and meet regulatory expectations. Our validation process includes risk assessment, documentation, testing, and lifecycle management.

SCADA, PLC & HMI Automation

Develop intelligent automation solutions for process monitoring, equipment control, alarm management, data logging, and secure operator interfaces.

Manufacturing Execution Systems (MES)

Optimize production operations with electronic batch records, recipe management, production monitoring, and real-time manufacturing visibility.

21 CFR Part 11 Compliance

Implement secure electronic records and electronic signatures with audit trails, role-based user access, password management, and complete data integrity.

Data Historian & Reporting

Capture, store, and analyze critical process data for regulatory compliance, production optimization, and performance reporting.

Laboratory & Instrument Integration

Integrate laboratory instruments and enterprise systems to improve traceability, automate data collection, and maintain accurate records.

Commissioning & Qualification

Support complete qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), ensuring systems are ready for production.


Key Features:

  • GAMP 5 compliant system implementation
  • Computer System Validation (CSV)
  • 21 CFR Part 11 compliance
  • Secure audit trails and electronic records
  • Role-based user access and security
  • Data integrity and cybersecurity
  • Real-time monitoring and reporting
  • Automated alarm and event management
  • Lifecycle documentation and validation support
  • Integration with PLC, SCADA, HMI, MES, ERP, and laboratory systems


Industries We Serve:

  • Pharmaceutical Manufacturing
  • Biotechnology
  • Life Sciences
  • Medical Devices
  • Healthcare
  • Food & Beverage
  • Cosmetics & Personal Care
  • Research Laboratories

Why Choose Us?

Our team combines automation expertise with regulatory knowledge to deliver reliable, scalable, and fully compliant solutions. From concept and design to validation, commissioning, and long-term support, we help manufacturers achieve operational excellence while maintaining the highest standards of quality and compliance.

Partner with us to build future-ready automation systems that improve efficiency, ensure regulatory compliance, and support sustainable manufacturing growth.