Autoscribe has released a new version of the Matrix Stability Express software for organising, tracking and reporting the results of pharmaceutical stability studies.
Autoscribe's Matrix Stability Express aids compliance with FDA 21 CFR Part 11 and comes with a suite of standard Crystal reports for stability operations.
This new version improves auditing of all stability operations for compliance purposes and has an easier, more flexible mechanism for tracking and recording the use of spare containers beyond those needed to execute the protocol.
There is an optional product release option that allows a release sample to be registered and tested, outside of the stability protocol.
This is important for customers that don't wish to or cannot justify implementing a full LIMS.
