The delivery of automation and MES systems is our core business and we have experience and expertise in project management, engineering and validation required to deliver solutions to specification, schedule, quality and cost.
We can deliver fully validated systems in the highly regulated life sciences industry or leaner solutions to the non-regulated sector. We have the flexibility to adjust to your industry and your requirements.
We have a proven track record delivering large and small, new and upgrade systems on both standalone and plant wide configurations. We are confident that our knowledge and experience will help make the more challenging undertakings less daunting.
We also have the expertise to build on the automation system and develop the MES layer or ERP system interface that will provide more sophisticated planning, tracking and reporting functionality. The methodology applied here is consisted with the S95 standard.
We are also fully acquainted with the S88 batching standard and have implemented many systems in accordance with this methodology. We can also provide engineering and validation expertise to help you with newer technologies such as PAT. Our experience in these and other specialist areas including security, audit trails, redundancy etc can be leveraged to ensure the design and implementation of your solution is solid and effective.
We have been engineering systems in accordance with GAMP for many years and have adopted our methodology to reflect the evolving guideline from GAMP3 through to the current GAMP5. Similarly GMP, GDP are also standard principles for us and we fully understand how these need to applied in your business.