White Paper

Cleanrooms are an essential part of production and research processes in numerous industries - from pharmaceutical and medical technology to semiconductor production. The demands on cleanrooms are high: they must meet standards such as ISO 14644, GMP or FDA specifications and at the same time be able to react to changing production requirements or new technologies. These continuous adaptation requirements often make the conversion of existing cleanrooms indispensable.

This white paper explains why cleanrooms are being converted and how this can be successfully implemented. It also presents a specific project example from pixon engineering AG, which was realized in 2024 for Solvias AG in Kaiseraugst. The aim is to provide a detailed insight into the challenges and solutions that need to be considered for a successful conversion.