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Cadar QS-Pro

New features in version 4

Home > Products > QS-Pro > Version 4

In the fourth major release of QS-Pro the emphasis is on traceability and compliance with the US FDA standard 21CFR part 11, but there are lots of improvements in other areas too - mostly in ease of use and flexibility.  Click on any of the sub- headings below for more information.


21CFR Part 11 Compatibility

Login Security

Integrated Batch Copying

Easy Batch Searching

Closed Batches and Templates

Elimination in Basic Batches

One Batch at a Time Operation

More Instrument Drivers

Upgrading Earlier Versions

Any company manufacturing products or components for use with drugs in the US market must operate a 21CFR compliant manufacturing environment in which the integrity of any and all data collected can be guaranteed.  QS-Pro can now operate in a 'signed' database where all batches are signed before use and all data is electronically signed by the operator at the point of measurement.

All users must login to QS-Pro with their own user name and password and any data they collect is tagged with their user name and signed so that it can't be changed later.

While you can still delete data this is retained for future reference and marked with a logbook message, the user name of the person deleting it and the time of deletion.

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