The Rotronic Monitoring System (RMS) is a GAMP©5 category 4 software combined with category 1 hardware, helping users monitor their GxP compliant applications, looking into the critical quality attributes and monitoring critical process parameters, helping focus on patient safety, product quality and data integrity and compliant to EudraLex Annex 11 and FDA 21 CFR Part 11.
With RMS, monitoring of any parameter is simple with the core RMS hardware, but 3rd party integration is also possible via analogue and MODBUS TCP signals. Integration and extraction of data is also possible with RMS’s application programming interface (API).
Designed with pharmaceutical companies for pharmaceutical companies, the user-friendly interface makes the monitoring so easy, that the user only has to focus on their main tasks.
Your main benefits:
Forget the hassle of having to maintain your IT infrastructure and focus only on what is crucial to your application. You can setup multiple measurement points in various locations and access the data from any device with a browser and internet connection. Setup alarms and notifications to be sure that you are always informed of what is happening!
Hosted on a high security and redundant datacentre with your own virtual server, you can run the Rotronic category 4 software in the cloud throughout each and every GxP compliant facility. Equip your worldwide facilities with the RMS hardware and access all of the data, including the audit trail, alarming and data analysis functions from a completely validated system.
Run the RMS software with an SQL database on your own IT infrastructure and have complete control over your entire system and comply to your own internal regulations, access the interface via most browsers.
For more information please contact us.