A Manufacturing System Designed Around Sterility
Our manufacturing facility in Bengaluru is structured to support the full lifecycle of sterile injectable production — from material staging and formulation through aseptic filling, inspection, and final release.
Each stage is governed by documented procedures and quality checkpoints, ensuring that sterility, potency, and product integrity are maintained without exception.
From Raw Material to Final Release
A validated, sequential workflow that maintains sterility and quality at every stage.
Material Intake & QC
Raw materials are received, quarantined, and tested before release into production.
Formulation
Precise compounding under controlled environmental conditions to specification.
Aseptic Filling
Validated aseptic filling lines maintain sterility through container closure.
Inspection & Release
100% visual inspection and quality review precede every batch release.
Quality Governance at Every Stage
Documented SOPs
Standard operating procedures govern every process step with full traceability.
In-Process Monitoring
Continuous environmental and process monitoring across sterile production zones.
Analytical Testing
Rigorous laboratory testing validates every batch against defined specifications.
Batch Release Review
Independent quality review and sign-off precede every product release.
Facility Built for Sterile Production
Our Bommasandra facility integrates classified clean room environments, controlled material and personnel flow, and dedicated utilities to support consistent sterile manufacturing.
Classified Clean Rooms
HVAC-controlled environments engineered to sterile manufacturing standards.
Controlled Flow Design
Dedicated material and personnel pathways to minimize contamination risk.
Dedicated Utilities
Purified water, compressed air, and HVAC systems built for pharmaceutical use.
Explore our product categories
See the sterile injectable categories manufactured at Sterig.