We are experts in the highly regulated pharmaceutical and biotech industries. Our efficiency is aided by the use of our software tools, which have been validated for use in FDA-regulated environments. We work together with our customers to design unique automation solutions and deliver systems that meet regulatory compliance while increasing efficiency.
MCS has the right technology, consultants and expertise to design and implement or support and maintain complex process control systems to enable your “bench to patient” goals. We support customers to develop flexible automated controls strategies during process development and pilot scale up, as well as implementing validated controls for clinical and commercial manufacturing.
MCS can leverage different industry proven software solutions that can collect, store, contextualize and visualize real-time time-series data. Connect all your machines, devices and computer systems into a centralized data architecture pattern to provide a single source of truth. Enable decisions by organizing your data with a standard naming structure that is meaningful to your business.
MCS follows global industry guidelines and good automated manufacturing practices to ensure that your computer systems are effective and of high quality, fit for intended use, and compliant with applicable regulations. Our goal is to focus on patient safety, product quality and data integrity with agile software development.