SmartScan can automatically generate a comprehensive batch report containing multiple processes for a pharmaceutical or medical device manufacturer.

Measurement data, including values, alarm status, and a timestamp can be easily exported to other systems using OPC (SmartScan acting as the server),

The SmartScan Validation Templates consist of four documents in Microsoft Word or PDF format. The documents have been designed to minimize the effort

Good manufacturing practices (GMP) are the practices required in order to conform to guidelines recommended by agencies that control authorization and

SmartScan is highly scalable from just a few monitoring points to thousands. Each numeric monitoring point can have a measurement value

SmartScan meets or exceeds the guidance published in FDA 21 CFR Part 11 which covers the security (preventing change) of data stored in electronic

Alerts in SmartScan can be sent by email, text message, pager, or voice telephone. Administrators can define exactly what an alert message will

A verity of easy to use data analysis tools are provided with the SmartScan system. Of these, the trend chart (plot of measurement values vs. time) is