Since December 2022, LOWTeqpdms has already been certified as a Class IIb medical device in accordance with the new Medical Devices Regulation (2017/745/EU).

LOWTeqpdms presents complex data in a clear and quickly accessible form, supporting the evaluation of patient condition and diagnosis. It relieves medical personnel of the burden of documentation and makes patient data available beyond just the bedside.

LOWTeqpdms can show doctors’ findings, history, care and medication documentation, therapy and care planning, and medication prescriptions. It thus acts as an electronic prescription system.

LOWTeqpdms is distinguished by its proven ease of use. The quality and functionality of the system has been confirmed in use throughout Europe.