Solutions
Sterile process systems, skids, and automation for pharmaceutical manufacturing
Five integrated solution lines, each custom-engineered around your process, fabricated in-house, factory tested, and qualified to regulated standards.
Vessels
Storage
Skids
Cleaning
Controls
What we build
One engineering partner for the whole process line
Esteril designs and builds custom sterile process equipment across five solution lines: manufacturing vessels, sterile holding vessels, complex process skids, CIP/SIP systems, and automation.
Each system is engineered around your product, utilities, batch sizes, and validation targets, then fabricated, tested, and qualified in-house. Systems integrate with WFI, PW, clean steam, and compressed air, and are built for cleanability and drainability, with contact parts electropolished to 0.3 Ra.
Our solutions
Engineered for every critical process
Fully integrated, factory-tested systems built to your specification and validated for faster installation.
Custom-engineered, multi-equipment skid systems for advanced pharmaceutical and biotech applications. Fully integrated and factory tested for faster installation.
Our Manufacturing Vessels and Skids offer fully integrated, customizable solutions for aseptic processes, ensuring designed for complete drainage and effective CIP/SIP cleaning.
Our Sterile Holding Vessels ensure safe liquid storage with designed for complete drainage and effective CIP/SIP cleaning, reliable automation, and rigorous testing, supporting capacities from 3 to 25,000 L.
Our CIP/SIP systems offer automated cleaning and sterilization for multi-tank setups, with custom, modular designs compliant with US FDA and cGMP standards.
PLC-SCADA automation systems for sterile and biopharma facilities, built to USFDA 21 CFR Part 11 and GAMP guidelines with electronic batch record integration.
Not sure which fits?
Tell us your process requirement
Share your line constraints and validation targets. We’ll scope the right system with you.
Tested before it ships
Proven at our facility, Then proven at yours
Every system is factory acceptance tested before dispatch, then site acceptance tested after installation. Our QA team prepares and maintains the required documentation through both phases, so validation and compliance are built in, not bolted on.
Dedicated FAT facility
Live testing of complete process systems under specified conditions before dispatch.
Orbital welding
Hygienic, repeatable welds with electropolished contact parts for contamination control.
On-site QA / QC lab
Material validation and quality checks carried out in-house through fabrication.
Full qualification docs
Structured DQ, IQ, OQ, and PQ documentation delivered with every system.