Solutions
SOLUTIONS
At Esteril Process Solutions, we recognize that developing solutions for any industry presents significant challenges. It requires not only a deep understanding of current conditions but also the foresight to implement future-proof technologies and processes. Through continuous improvement and innovation, we provide smarter, more efficient solutions tailored to our clients’ evolving needs.
Our enduring values, extensive knowledge, and generations of experience, combined with a commitment to refining our processes, enable us to address customer requirements with greater effectiveness and precision.
Esteril Process Solutions specializes in creating tailor-made solutions for unique challenges, empowering companies to adopt cutting-edge technologies and processes. We are dedicated to delivering the highest quality products and world-class service, helping our customers make a global impact and improve countless lives.
FACTORY ACCEPTANCE TEST (FAT) / SITE ACCEPTANCE TEST (SAT)
All our systems undergo rigorous testing in our dedicated FAT (Factory Acceptance Testing) area, fully equipped with all necessary utilities. We ensure that every instrument performs optimally under the specified conditions, providing reliable and efficient results.
Our quality assurance (QA) team meticulously oversees the entire process, ensuring that all required documentation is thoroughly prepared and maintained before and during the FAT/SAT (Site Acceptance Testing) phases. This attention to detail guarantees smooth validation and compliance, delivering systems that meet the highest industry standards.
High Quality Products & World Class Service
Our Manufacturing Vessels and Skids offer fully integrated, customizable solutions for aseptic processes, ensuring 100% cleanability and drainability.
Our Sterile Holding Vessels ensure safe liquid storage with 100% cleanability, reliable automation, and rigorous testing, supporting capacities from 3 to 25,000 liters.
Custom-engineered, multi-equipment skid systems for advanced pharmaceutical and biotech applications. Fully integrated and factory tested for faster installation.
PLC-SCADA automation systems for sterile and biopharma facilities, built to USFDA 21 CFR Part 11 and GAMP guidelines with electronic batch record integration.
Our CIP/SIP systems offer automated cleaning and sterilization for multi-tank setups, with custom, modular designs compliant with US FDA and cGMP standards.
