All service work completed by iLab Solutions uses a defined protocol which is determined by risk assessments for both the customer's system and other known service records. If you prefer to complete your own service protocols we can provide the documentation required. These revision-controlled cGMP documents are based upon continually evolving best practices.
We'll perform a physical review adopting an FMEA approach and consider all the major functional areas of the equipment. This will identify all potential points of exposure and include maintenance frequency, personal training, spare parts strategies and operational procedures.
iLab Solutions will work with you to establish a quote based on the specificity of the equipment and your needs. For example, type of equipment, type of production, type of product, process steps, product stability, spare parts, people competencies. We will establish a process that ensures the capital investment you have made in your process scale chromatography is properly maintained for optimum system performance and longevity.