<< Click to Display Table of Contents >> Navigation:  »No topics above this level« Introduction to the Rotronic Monitoring System

The Rotronic Monitoring System 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 EU Annex 11 and FDA CFR 21 Part 11. Rotronic AG design and manufacture RMS hardware and software based upon the GAMP©5 guidelines.

 

The Rotronic continuous Monitoring System allows user to monitor anything from anywhere using an On-Premise or SaaS - Public Cloud software solution. Rotronic offer an SaaS - Exclusive Cloud option for any regulated customer that needs a validation SaaS software solution.

 

Find out more in our short explain it movie.

 

Specific chapters concerning RMS:

•Data Security, Integrity & Data Availability.

•RMS Software Solution Overview.

•RMS Software Compliance.

•RMS Diagrams.

•Data Import and Data Export.

•Integrating RMS with other Systems.

 

Access the main chapters of the online manual:

•Software Overview.

•Hardware Overview.

•Service Overview.

•Quick Start.

•Help.

 

The RMS software is translated to following languages:

•English,

•Bulgarian,

•Croatian,

•Hungarian,

•Czech,

•Finnish,

•German,

•Turkish,

•French,

•Italian,

•Spanish,

•Russian,

•Dutch,

•Chinese (simplified),

•Japanese,

•Polish,

•Portuguese.

If one of these is chosen as browser language, RMS will be in that language.

If another one is chosen as browser language, RMS will be shown in English.

 

Pop up windows may be selected and moved.

 

For any direct enquiries, please contact rms@rotronic.ch.

 

Updated: 19.11.2024.