Sterile Vessel is made as per WHO & USFDA standards of manufacture sterile solutions. It is available in various configuration with instrumentation from manual operation to full automation. it is designed and fabricated as per ASME BPE & EHEDG guideline to meet cGMP & USFDA requirement.
Application
We design an automation system that is reliable, easy to operate, connects and sequences the processes seamlessly. Our system design ensures different equipment’s work together in proper sequence.
Automation that is driven by highly reliable and accurate instruments and controls deliver consistency and repeatability. A highly skilled, experienced and well trained electrical & automation team works together with process specialists to design automation sequences that are implemented and rigorously tested.
The cleaning characteristics of Sterile vessels are key right from the start of the design process. It is essential to eliminate dead-leg areas and ensure that Clean-in-Place (CIP) and Sterilize-in-Place (SIP) systems are effective.
Cleaning capability is then verified in practice, using a Riboflavin test, for every vessel supplied.
Throughout the manufacturing process, all vessels are subject to stringent quality checks. An overall test forms part of the FAT (Factory Acceptance Tests) procedures and the relevant documentation forms part of the FAT protocols.
Our quality system ensures the full traceability of all materials used including the provision of certificates.
