A focus on documentation, safety, and validation
Enterprise Automation can help with your next validated install in a GMP environment, and will ensure the proper processes and testing are utilized to achieve the highest quality possible.
The Life Science industry is all about safety and high quality. EA believes that these should be highest priority in every industry, and has always produced control systems with this in mind. Our design, development, and testing methodologies are second to none and allow for repeatable results on project after project.
Give us a call & ask how we can help.
Integration is 10% of the project cost and 75% of the risk.
Here's how we remove the risk.
1. Detailed Design & Documentation
2. Proactive Project Management
3. Nothing Leaves Enterprise Untested
As the final stopgap to removing project risk, everything we do and develop is thoroughly tested prior to leaving our offices. Our promise to clients is that startup in the field will be about validating that the physical installation can execute the controls process defined during the design phase of a project. When EA arrives on site, we know the programming is 100% complete, and that it does what stakeholders have specified. As a result, startups are quick and smooth. This reduces costs associated with having multiple trades on site, and lost revenue from extended downtime.