Systematix customers benefit from the disciplined approach and expertise gained through engineering hundreds of automated assembly and test systems for the Life Sciences.
We build quality into all areas of the engineering, assembly and integration processes. Understanding production needs from cleanroom, vision inspection, specialized handling and robotics to defect segregation and functional testing, we have you covered.
We can ease you into your automation journey with process development solutions. We have many ways to mitigate your pain points while adding value to your new process with experienced pre-automation planning to proof of principle studies, prototyping, simulations, and cycle time analysis.
To help reduce the risk and cost associated with new product launches, Systematix is capable of semi-automated modular solutions that are value engineered and can scale up as your production volume or demand grows. Scale-up increases the batch size from lab to commercial scale, with each project having its own set of challenges. Developing an effective and successful scale up process is an art that not every manufacturing partner has mastered. As your partner, you can rely heavily on our experience, knowledge, and automation process capabilities. Flexibility and innovation are not only critical to new product developments but central to who we are.
A Systematix engineered turnkey automation system for high volume production is an extension of your quality management program. Our engineers integrate inline test, inspection, and process monitoring technology that allows you to run at rate while delivering reliable and accurate production and process data with 100% inspection and test of your critical processes. Utilizing industry standard vision technology or our own MAVIX software we provide inline inspection of incoming parts for defects, vision guided part orientation, assembly process confirmation, particle inspection, and reject identification at any stage of your manufacturing operation.
Systematix is ISO 9001:2015 certified and follows the controlled procedures and documentation recommended by Good Automated Manufacturing Practice (GAMP 5® guidelines) and FDA validation processes. Our controls designers and programmers are experts at integrating industry leading inspection, test, and process monitoring, configured to support industry regulatory standards. From testing to documentation, our validation protocols assure consistency, traceability, quality and compliance to manage risk in the highly regulated environments of the Life Sciences.