Our documentation starts in the factory and supports each piece of equipment throughout its life cycle. No other method of documentation is more accurate or efficient. STERIS and our preferred team of validation consultants will work to understand your process-specific documentation needs to provide protocols that complement your existing documentation formats.
Installation Qualification (IQ)
Operation Qualification (OQ)
Process Qualification (PQ)
Eliminates the guesswork in VHP cycle development, biological indicator testing and application troubleshooting.