Designing pharmaceutical and biological manufacturing facilities requires uncommon attention to detail, and the documentation to go with it. Our bio/pharmaceutical clients appreciate the hands-on pharma experience Sys-Tek’s team brings to the table. Our project documentation has become the standard that is used for all future projects for some of our clients.
At Sys-Tek, we have all the right skills to make a bio/pharmaceutical project succeed. Our team can help you size, select, and specify process equipment, including process vessels, packaging equipment, process utilities, cleaning equipment, and sterilization equipment. In addition, our knowledge of process controls and integration enables Sys-Tek to provide the quality documentation and specifications that ensure successful design, implementation, commissioning, and validation of these systems. Our recent projects include a 3200L bioreactor train, 5000L fermenter systems, downstream processing, CIP system expansion, and process waste optimization.
We have broad experience in providing clean and safe manufacturing environments that are required for bio/pharmaceutical operations. From Class A through Class D clean rooms, bio-safety level 1 through 3 containment, and potent compound containment and ventilation, our designs include all necessary provisions to ensure that the quality and safety of these environments are maintained.
To discuss your project or for further information, please contact us.
We look forward to hearing from you!