The software has its focus on laboratory workflows, with a rule engine and a comprehensive communication module. PTA supports the manufacturer in eliminating identified weaknesses and in implementing improved or newly added functions. Activities in the areas of analysis, implementation and validation are carried out. The agile development process is managed largely autonomously.
The software serves as the central control unit for the laboratory workflow, but also enables areas such as sample acquisition or technical and medical validation, organised with role-based access. Important technical areas such as clinical chemistry including haematology or PCR, or microbiology or blood banks are supported. For quality control, rules according to Westgard and/or the Average of Normals (monitoring of laboratory measuring stations by tracking the inconspicuous patient readings) can be included.