· PURPOSE·
· LIFE SCIENCES & PHARMACEUTICAL PRODUCTION ·
· SMARTER MANUFACTURING FOR LIFE SCIENCES ·
· Engineering Precision, Ensuring Patient Safety ·
Automation That Scales With Science
At Automation-IT, we deliver precision-engineered solutions that help pharmaceutical and biotech manufacturers boost efficiency, ensure compliance, and maintain the highest levels of product quality.
We bring digital transformation to every step of your process.
· AUTOMATION BUILT FOR PHARMA AND BIOTECH ·
We design GMP enabled systems ready to be integrated in your QMS. Our systems ensure seameless integration
in your quality management system ensuring and easy and painless validation process.
· AUTOMATION THAT POWERS ·
EVERY PHASE OF DRUG PRODUCTION
At Automation-IT, we specialize in precision automation for pharmaceutical and biotech operations
helping manufacturers optimize yield, reduce risk, and enhance data integrity.
Our automation strategies empower your team to increase throughput
while ensuring quality, traceability, and regulatory compliance.
· OUR SYSTEMS BRING SMART AUTOMATION TO EVERY STAGE: ·
· BIOREACTOR ·
CONTROL
DELIVERS PRECISE CONTROL OF CRITICAL PARAMETERS
FOR OPTIMAL FERMENTATION OR CELL CULTURE.
· KEY FEATURES ·
- Closed-Loop PID Control Maintains tight control of pH, DO, agitation, temperature, and pH.
- Real-Time Process Analytics Integrated sensors for pH, DO, glucose.
- Automated Nutrient & Gas Feeding Based on processfeedback.
- Recipe-Based Batch Management Compliant with ISA 88 and 21 CFR Part 11.
- Monitoring & Alarms – SCADA/HMI access with audit trail.
- Seamless Integration with Downstream Processing Units.
- Secure Data Storage Compliant with ALCOA+ principles.
- Historical Trending & Root Cause Analysis.
· KEY FEATURES ·
- Gradient Control Automated buffer mixing.
- Pressure & Flow Regulation Ensures optimal column conditions and prevents fouling.
- Automated Column Switching Supports continuous or batch mode.
- CIP/SIP Integration Sanitizes between runs with validated cycles.
- Data Logging for Traceability Full audit trail for FDA/EMA inspection readiness.
· CHROMATOGRAPHY & FILTRATION ·
AUTOMATION
Purification precision
· PURPOSE·
Automates column packing, buffer exchange,
and concentration steps for maximum yield and purity.
· CIP/SIP AUTOMATION ·
VALIDATED CLEANING & STERILIZATION
· PURPOSE·
Ensures repeatable and compliant cleaning
and sterilization of bioprocess equipment.
· KEY FEATURES ·
- Customizable Cleaning Sequences Compliant with FDA and EMA guidelines
- Real-Time Monitoring of Flow, Temp & Conductivity
- Chemical Dosing Accuracy ±0.5% for detergents and sanitizers.
- Automated Documentation CFR 21 Part 11 audit-ready reports.
- Water & Energy Optimization Up to 30% reduction in resource consumption.
· KEY FEATURES ·
- Closed-Loop Control Monitors and adjusts variables in real time.
Integrated Temperature Control Maintains optimal conditions for product stability. - Scalable Recipes From lab scale to production batches.
- Automated Cleaning Protocols Reduces downtime and contamination risk.
- Batch Reporting Detailed logs for regulatory compliance and quality assurance.
· FORMULATION – MIXING ·
& HOMOGENIZATION AUTOMATION
Consistency in Every Batch
· PURPOSE·
Ensures uniform blending of active ingredients and
excipients with automated control over mixing speed, time, and temperature for consistent formulation results.