The PCR.AI device manager has a similar feature set to the PCR.AI workbench, but does not include access to the AI API by default.

It is designed for use with sample to answer tests that include curve-analysis, but still require advanced features such as data-management, LIMS integration, real-time monitoring of multiple platforms simultaneously, QA or periodic reporting, alerts, etc.

The system also enables laboratories to clearly document modifications to off-the-shelf tests, such as adjustments of CT ranges for new sample types or others based on in-house validations and issue resolutions or additions of new result reports.

Access to the CE-IVDR certified PCR.AI API can be integrated for requested assays such as LDTs or those that are not giving reliable results and a 'extra check' is warranted.

The PCR.AI Device Manager includes tools for laboratory documentation and validation of any SOP rules (new result types, repeat management, advanced Westgard checks, etc).

It is intended to assist qualified laboratory personnel in the management and review of PCR test results within clinical laboratory settings. The software automatically applies user-defined rules (such as cycle threshold [CT] value thresholds or quality control criteria) to flag results that require further human review. Flagged results may be configured to be held for manual assessment by laboratory staff before release to the laboratory information management system (LIMS). The PCR.AI Device Manager is intended solely as a workflow support tool to facilitate laboratory quality control and result management processes.