GMP Automation and Validation Specialists

In the pharmaceutical and biotech industry, we operate under strict GMP guidelines, offering a wide range of services including the design and programming of DCS or PLC+SCADA based control systems, equipment qualification, management and execution of the full cycle of CSV validations, and process engineering.

Our projects cover a wide range of features and dimensions, and we are able to automate, qualify and validate complete plants in any country. We strive to establish long-term relationships with our customers, prioritising customer satisfaction and excellence in every project we undertake.

We have a highly specialised team in the pharmaceutical industry, working under strict GMP guidelines, complying with CFR21 part 11 and EU Annex 11 following GaMP 5, ISA88, ISA101 guidelines. We have extensive experience in automation with various control systems, both DCS and PLC and SCADA, as well as in process engineering, equipment qualification and management and execution of the full cycle of CSV validations. We adapt to different scales, including large international projects ranging from automation to qualification and CSV validation of new production plants.