Epitome Technologies Pvt. Ltd. provides single point responsibility to solutions for plant automation with specialization in GAMP (Good Automated Manufacturing Practices) and US FDA 21 CFR Part 11 compliance for pharmaceutical industry. Epitome’s comprehensive strength of process engineering emerging technologies and regulatory compliance to the international guidelines makes it a partner with a unique blend of diverse expertise; ensuring successful implementation of computerized system project, from concept to compliance. Over and above, we have specialized in various activities.

Epitome has a rich experience of delivering the Project Objectives to the utmost satisfaction of the customer. Due to our high tech Resources and Facilities we get Repeat Business,  from our existing customers and the continuously expanding client base.

WHY EPITOME?
Team of Experienced Professionals
Excellent Track Record for Project Execution
Vast Experience in Meeting International Regulatory Compliance
Strategic Alliances with Leading Organizations
Exposure To Various Industries
Optimum System Recommendations
Accurate Engineering
Audit Clearance experience of US FDA, MHRA, MCC, TGA, UNICEF, DMA etc.




Process Automation
Process/API Automation
GAMP based Validation
US FDA 21 CFR Part 11 compliance services
BMS Automation
PLC/DCS / BMS / SCADA Validation
SAP R/3 Software Validation
ERP Validation
Laboratory Instruments Software Validation
Gap / Impact Analysis, Risk Assessment



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