FAQ - Pharmaceutical/Life Sciences Particle Counting

Facility Monitoring Software: PharmaceuticalNet

Question
What do we need to do to validate the software for use in a Pharmaceutical GMP environment?

Answer

There are two parts to the validation process. First, the software is validated internally at Particle Measuring Systems. Second, after the monitoring system has been installed in your facility and the software is configured to interface with the hardware in your facility, your specific software configuration will require IQ/OQ validation. We can provide validation services for our software and monitoring systems. Please let me know if we can assist you.