HEALTH ///
Proactive risk management is a legally binding obligation for IT networks in the medical technology environment.
CRISAM® supports you in implementing these requirements.
WITH CRISAM® YOU CAN MEET THE REQUIREMENTS OF THE DIGITALIZATION OF THE HEALTHCARE INDUSTRY
With the increasing digitalization of computer-assisted medical devices and the ever-increasing security requirements against cyber-attacks, the security and reliability of medical device networks is of central importance.
More and more medical devices are connected to the hospital IT network. The reason for this is the rapid development of the entire information technology – and the associated desire for faster transmission for receiving, sending patient data, as well as monitoring the devices themselves. Due to the resulting high responsibility of the network operator in healthcare facilities with medical devices, it is necessary to have a structured and professional risk management. The IEC 80001-1 standard and EN ISO 27799 underscore the need that has arisen in this context.
>> WITH CRISAM® YOU CAN PROFESSIONALLY IMPLEMENT
THE INDUSTRY-RELEVANT STANDARDS IEC 80001-1 AND EN ISO 27799 <<
IDENTIFY AND ASSESS RISKS WITH CRISAM®
With CRISAM® you assess risks both as deviations from technical, organizational and normative references and with relevance to your organization. CRISAM® optimally supports you in implementing and operating an effective, resource-saving and certified information security and risk management process.
Risks are identified and evaluated using the fault tree analysis included in CRISAM® in accordance with DIN 25424. This makes the causes and effects immediately recognizable.
Deviations from the standard requirements and the state of the art are immediately displayed in the software and as a report. Necessary measures to deal with the risks are only a few clicks away thanks to the recommended measures included in the CRISAM® Content Libraries.
