Interface to Dosage Management Systems
Implementation of the EURATOM Directive
Streamlined processes through an optimal integration into your workflow
The European EURATOM directive wants to further improve the radiation protection at the workplace for the general public and the medical radiation protection. The directive is based on the most recent scientific standard and its goal is to ensure a comprehensive protection from ionizing, i.e. high-energy radiation.
The directive has to be implemented into national law until February 6, 2018.
medavis offers its users the possibility to connect any external Dosage Mangement System to medavis RIS in the future via an interface.
The connection enables both the automated integration of the dosage values from the Dosage Management System into the radiological report and also the call of an external Dosage Management System on examination and patient level. The call will be supported from reporting and also other medavis RIS pages.
With the medavis interface to an external Dosage Management System you are on the safe side
Your advantages with the medavis interface to a Dosage Management System
Complete integration in your medavis RIS workflow without additional effort during reporting
Automated integration of the dosage values into the radiological report via a respective placeholder in the report templates
Call of an external Dosage Management System on examination and patient level directly from reporting
With the medavis interface to an external Dosage Management System you are on the safe side
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Do you have further questions or would like to get a demo?
Do not hesitate to contact us. We look forward to providing you with the necessary advice or to arrange a demo appointment with you, in order to present your optimal workflow.