A proactive risk management approach is a legally binding obligation for IT networks in the medical technology environment. CRISAM® assists you in implementing these requirements.
Request nowWith the increasing digitization 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 all 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 health care facilities with medical devices, it is necessary to operate a structured and professional risk management. The IEC 80001-1 and EN ISO 27799 standards underline the need that has arisen in this context.
With CRISAM® you can implement the industry-relevant IEC 80001-1 and EN ISO 27799 standards professionally.
With CRISAM® you assess risks both as a deviation 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 assessed 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 actions to address the risks are now just a few clicks away through the recommended actions included in the CRISAM® Content Libraries.
