Life is too short for poor batch implementations. Many organizations are purchasing equipment—especially bioreactors—with an inappropriate batch philosophy, resulting in
Smart Manufacturing
Modular, scalable designs to tightly integrate the process controllers and operator interfaces are our specialty.
Our goal is to meet performance requirements while also building in reduced total ownership cost: testing, maintenance, and future capacity.
S88 Batch
Defining an S88 model for your equipment and processes frees the flow of data between the business requirements and discrete automation control.
Quality control, batch analysis, and logging of process execution is the first step to feedback best practices for increased production.
Validation
Reduce validation testing time by automating test generation and execution.
Our experience in regulated environments results in designs mindful of validation upfront. Maintain traceability from design, code development, to operational qualification.
Reduce the time and effort to secure and validate processes and data integrity with our technology to reduce entire design process from User Requirements to Operational Qualification. Maintain both design and validation documents in a single database. Changes to the design are automatically updated in the requirements specification, test forms, and audit log.
Extensive experience integrating Rockwell Allen-Bradley PLCs, FactoryTalk View SE SCADA systems, RS Batch, iBatch, iFix, Wonderware, Archestra System Platform, and Inductive Automation will deliver the system to fit your need.
Life is too short for poor batch implementations. Many organizations are purchasing equipment—especially bioreactors—with an inappropriate batch philosophy, resulting in
Finally got the go-ahead to upgrade a system I installed back in 2014, and the results are sweet. Zero downtime, more
GMP compliance is time-consuming, don’t make it harder with a bolt-on solution. A turnkey system designed for easy documentation, validation,
In GMP life sciences, upgrades are tricky with all the legacy validation to consider. Swapping out a reporting solution, the
Single-use systems get a bit of a bad rap. Not so much for the equipment itself, but because of the
No equipment exists on an island. Sooner or later, process data and audit logs must connect to your facility’s infrastructure.
In the ever-evolving world of automation, particularly in biotech and pharma manufacturing, hands-on experience and continuous learning are invaluable. To
Our engineering team had a great time at ISPE Vendor Night. Not only highlighting the latest technologies, but served as
Life is too short for poor batch implementations. Many organizations are purchasing equipment—especially bioreactors—with an inappropriate batch philosophy, resulting in