Clinical Rules focuses primarily on drug safety. It provides support for writing and monitoring (repeat) prescriptions, for example when lab reports become available, a patient reaches a certain age limit or when a new diagnosis is made. This monitoring process is made possible through a collaboration with your Health Care Information System (XIS) provider, in which anonymised data are exchanged with the Clinical Rules Engine. The Clinical Rules Engine detects potential problems and reports these back to the XIS.
This makes Clinical Rules the next step in drug safety: as an instrument, it is quality enhancing, reliable, time-saving, efficient, more specific, more intuitive to use, easy and well-organised.