Pharma Upgrade
21 CFR Part 11
Compliant
Industry 4.0 Transformation

Integrity Driven Upgradation

The digital industrial revolution is here, and it's fueled by up-gradation. Ensuring compliance with 21CFR Part11 is essential in the modern pharmaceutical and biotech industries, where maintaining the integrity of digital records is paramount.

What We Offer ?

Retrofitting & Upgradation

We offer specialized upgradation and retrofitting solutions for Tablet Presses, FBD, RMG, Coaters, Blenders, Blister Pack Machines, Autoclaves, and Water Systems.

  • Legacy Machine Modernization
  • Extended Equipment Life

Smart L1 Integration

Increased functionality by integrating PLC, HMI, and SCADA systems to support features such as Batch Summaries, Alarms, and Audit reporting with advanced AI tools and customized security.

  • AI Batch Summaries
  • Seamless Data Flow

Regulatory Framework

Our systems are designed to fully comply with all global regulatory requirements, specifically 21 CFR Part 11 and GAMP 5, ensuring audit-ready operations.

  • Validation Documentation
  • Audit-Ready Logs

Data Integrity & Security

We ensure accuracy, completeness, and consistency in data generation and maintenance, building a secure framework for electronic records and seamless data transfer.

  • Role-Based Access
  • Encrypted Data Vaults